A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516912



Internal ID15444205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54464430..54483031hg38UCSC Ensembl
Innerchr15:54756628..54775229hg19UCSC Ensembl
Innerchr15:52543920..52562521hg18UCSC Ensembl
Innerchr15:52543920..52562521hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3818602
hg1918602
hg1818602
hg1718602
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv148n21
Supporting Variantsnssv690211, nssv673894, nssv684593, nssv654914
Samples
Known GenesUNC13C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516912
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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