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dbVar

Database of genomic structural variation

nsv498730

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:20,709

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: 174 SVs from 44 studies. See in: genome view

Remapped(Score: Perfect):67,566,136-67,586,844

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv498730	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	67,566,136	67,586,844
nsv498730	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	69,325,894	69,346,602
nsv498730	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000010.9	Chr10	68,995,900	69,016,608

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585447	copy number loss	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585447	Remapped	Perfect	NC_000010.11:g.675 66136_67586844del	GRCh38.p12	First Pass	NC_000010.11	Chr10	67,566,136	67,586,844
nssv585447	Remapped	Perfect	NC_000010.10:g.693 25894_69346602del	GRCh37.p13	First Pass	NC_000010.10	Chr10	69,325,894	69,346,602
nssv585447	Submitted genomic		NC_000010.9:g.6899 5900_69016608del	NCBI36 (hg18)		NC_000010.9	Chr10	68,995,900	69,016,608

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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