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dbVar

Database of genomic structural variation

nsv4579937

Organism: Homo sapiens

Study:nstd183 (DECIPHER Consensus CNVs)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,566

Links to Other Resources

Overlapping Genes

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: 173 SVs from 24 studies. See in: genome view

Remapped(Score: Perfect):186,312,380-186,313,945

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4579937	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	186,312,380	186,313,945
nsv4579937	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	186,281,512	186,283,077

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16098712	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16098712	Remapped	Perfect	NC_000001.11:g.(?_ 186312380)_(186313 945_?)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	186,312,380	186,313,945
nssv16098712	Submitted genomic		NC_000001.10:g.(?_ 186281512)_(186283 077_?)del	GRCh37 (hg19)		NC_000001.10	Chr1	186,281,512	186,283,077

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16098712	0.001	1	845

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