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dbVar

Database of genomic structural variation

nsv7098542

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:73

Description:NC_000023.10:g.(?_64196185)_(64196257_?)del AND not provided

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: 107 SVs from 20 studies. See in: genome view

Remapped(Score: Perfect):64,976,305-64,976,377

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv7098542	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	64,976,305	64,976,377
nsv7098542	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	64,196,185	64,196,257

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv18787005	deletion	Multiple	Multiple	not provided	Pathogenic	ClinVar	RCV003119923.2, VCV002426481.2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18787005	Remapped	Perfect	NC_000023.11:g.(?_ 64976305)_(6497637 7_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	64,976,305	64,976,377
nssv18787005	Submitted genomic		NC_000023.10:g.(?_ 64196185)_(6419625 7_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	64,196,185	64,196,257

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
nssv18787005	GRCh37: NC_000023.10:g.(?_64196185)_(64196257_?)del	deletion	germline	not provided	Pathogenic	ClinVar	RCV003119923.2, VCV002426481.2

No genotype data were submitted for this variant

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