A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661102



Internal ID15397754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24366837..24540053hg38UCSC Ensembl
Innerchr15:24611984..24785200hg19UCSC Ensembl
Innerchr15:22163077..22336293hg18UCSC Ensembl
Innerchr15:22163077..22336293hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38173217
hg19173217
hg18173217
hg17173217
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517191
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661102
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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