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dbVar

Database of genomic structural variation

nsv7097611

Organism: Homo sapiens

Study:nstd102 (Clinical Structural Variants)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: Yes
Region Size:438,363

Description:NC_000007.13:g.(?_144094333)_(144532695_?)del AND Childhood encephalopathy due to thiamine pyrophosphokinase deficiency

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 1166 SVs from 79 studies. See in: genome view

Remapped(Score: Perfect):144,397,240-144,835,602

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7097611	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	144,397,240	144,835,602
nsv7097611	Remapped	Pass	GRCh38.p12	PATCHES	Second Pass	NW_018654715.1	Chr7\|NW_01 8654715.1	446,707	680,662
nsv7097611	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	144,094,333	144,532,695

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18789447	deletion	Multiple	Multiple	Childhood encephalopathy due to thiamine pyrophosphokinase deficiency; THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE); THMD5; Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)	Pathogenic	ClinVar	RCV003111492.2, VCV002426756.3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18789447	Remapped	Pass	NW_018654715.1:g.( ?_446707)_(680662_ ?)del	GRCh38.p12	Second Pass	NW_018654715.1	Chr7\|NW_01 8654715.1	446,707	680,662
nssv18789447	Remapped	Perfect	NC_000007.14:g.(?_ 144397240)_(144835 602_?)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	144,397,240	144,835,602
nssv18789447	Submitted genomic		NC_000007.13:g.(?_ 144094333)_(144532 695_?)del	GRCh37 (hg19)		NC_000007.13	Chr7	144,094,333	144,532,695

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	HGVS	Type	Allele Origin	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18789447	GRCh37: NC_000007.13:g.(?_144094333)_(144532695_?)del	deletion	germline	Childhood encephalopathy due to thiamine pyrophosphokinase deficiency; THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE); THMD5; Thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)	Pathogenic	ClinVar	RCV003111492.2, VCV002426756.3

No genotype data were submitted for this variant

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