A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706040



Internal ID15442692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23448259..23547626hg38UCSC Ensembl
Innerchr15:23693406..23792773hg19UCSC Ensembl
Innerchr15:21244499..21343866hg18UCSC Ensembl
Innerchr15:21244499..21343866hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3899368
hg1999368
hg1899368
hg1799368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522641
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706040
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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