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dbVar

Database of genomic structural variation

nsv4456647

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:409,009

Description:GRCh37/hg19 8p22(chr8:17474031-17883039)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: 1949 SVs from 96 studies. See in: genome view

Remapped(Score: Perfect):17,616,522-18,025,530

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4456647	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	17,616,522	18,025,530
nsv4456647	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	17,474,031	17,883,039

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15776530	copy number loss	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV000849488.2, VCV000688797.2	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15776530	Remapped	Perfect	NC_000008.11:g.(?_ 17616522)_(1802553 0_?)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	17,616,522	18,025,530
nssv15776530	Submitted genomic		NC_000008.10:g.(?_ 17474031)_(1788303 9_?)del	GRCh37 (hg19)		NC_000008.10	Chr8	17,474,031	17,883,039

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
nssv15776530	GRCh37: NC_000008.10:g.(?_17474031)_(17883039_?)del	copy number loss	unknown	not provided	Uncertain significance	ClinVar	RCV000849488.2, VCV000688797.2	1

No genotype data were submitted for this variant

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