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dbVar

Database of genomic structural variation

nsv498886

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:21,675

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: 581 SVs from 64 studies. See in: genome view

Remapped(Score: Perfect):67,628,336-67,650,010

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv498886	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	67,628,336	67,650,010
nsv498886	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	65,295,573	65,317,247
nsv498886	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000018.8	Chr18	63,446,553	63,468,227

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585747	copy number loss	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585747	Remapped	Perfect	NC_000018.10:g.676 28336_67650010del	GRCh38.p12	First Pass	NC_000018.10	Chr18	67,628,336	67,650,010
nssv585747	Remapped	Perfect	NC_000018.9:g.6529 5573_65317247del	GRCh37.p13	First Pass	NC_000018.9	Chr18	65,295,573	65,317,247
nssv585747	Submitted genomic		NC_000018.8:g.6344 6553_63468227del	NCBI36 (hg18)		NC_000018.8	Chr18	63,446,553	63,468,227

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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