Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6637608

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:2,101,172

Description:GRCh37/hg19 15q25.1-25.2(chr15:79996626-82097796)x1 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: 4885 SVs from 96 studies. See in: genome view

Remapped(Score: Perfect):79,704,284-81,805,455

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6637608	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	79,704,284	81,805,455
nsv6637608	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	79,996,626	82,097,796

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv18330842	copy number loss	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV002472703.1, VCV001807897.1	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18330842	Remapped	Perfect	NC_000015.10:g.(?_ 79704284)_(8180545 5_?)del	GRCh38.p12	First Pass	NC_000015.10	Chr15	79,704,284	81,805,455
nssv18330842	Submitted genomic		NC_000015.9:g.(?_7 9996626)_(82097796 _?)del	GRCh37 (hg19)		NC_000015.9	Chr15	79,996,626	82,097,796

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
nssv18330842	GRCh37: NC_000015.9:g.(?_79996626)_(82097796_?)del	copy number loss	unknown	not provided	Uncertain significance	ClinVar	RCV002472703.1, VCV001807897.1	1

No genotype data were submitted for this variant

You are here: NCBI