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dbVar

Database of genomic structural variation

nsv499166

Organism: Homo sapiens

Study:nstd47 (Kidd et al. 2010b)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,097

Publication(s):Kidd et al. 2010

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: 354 SVs from 49 studies. See in: genome view

Remapped(Score: Perfect):131,680,790-131,681,886

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499166	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	131,680,790	131,681,886
nsv499166	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	131,550,684	131,551,780
nsv499166	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000011.8	Chr11	131,055,894	131,056,990

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585604	copy number gain	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585604	Remapped	Perfect	NC_000011.10:g.131 680790_131681886du p	GRCh38.p12	First Pass	NC_000011.10	Chr11	131,680,790	131,681,886
nssv585604	Remapped	Perfect	NC_000011.9:g.1315 50684_131551780dup	GRCh37.p13	First Pass	NC_000011.9	Chr11	131,550,684	131,551,780
nssv585604	Submitted genomic		NC_000011.8:g.1310 55894_131056990dup	NCBI36 (hg18)		NC_000011.8	Chr11	131,055,894	131,056,990

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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