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dbVar

Database of genomic structural variation

nsv4613610

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:130

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: 94 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):45,922,732-45,922,861

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4613610	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	45,922,732	45,922,861
nsv4613610	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	45,944,283	45,944,412

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16130700	duplication	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16130700	Remapped	Perfect	NC_000011.10:g.(?_ 45922732)_(4592286 1_?)dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	45,922,732	45,922,861
nssv16130700	Submitted genomic		NC_000011.9:g.(?_4 5944283)_(45944412 _?)dup	GRCh37 (hg19)		NC_000011.9	Chr11	45,944,283	45,944,412

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)
nssv16130700	0.008	7	845

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