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dbVar

Database of genomic structural variation

nsv6638024

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:296,790

Description:GRCh37/hg19 17p13.1-12(chr17:10517286-10814075)x3 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: 951 SVs from 66 studies. See in: genome view

Remapped(Score: Perfect):10,613,969-10,910,758

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6638024	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	10,613,969	10,910,758
nsv6638024	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	10,517,286	10,814,075

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv18330833	copy number gain	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV002472694.1, VCV001807888.1	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18330833	Remapped	Perfect	NC_000017.11:g.(?_ 10613969)_(1091075 8_?)dup	GRCh38.p12	First Pass	NC_000017.11	Chr17	10,613,969	10,910,758
nssv18330833	Submitted genomic		NC_000017.10:g.(?_ 10517286)_(1081407 5_?)dup	GRCh37 (hg19)		NC_000017.10	Chr17	10,517,286	10,814,075

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	Copy number
nssv18330833	GRCh37: NC_000017.10:g.(?_10517286)_(10814075_?)dup	copy number gain	unknown	not provided	Uncertain significance	ClinVar	RCV002472694.1, VCV001807888.1	3

No genotype data were submitted for this variant

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