A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516347



Internal ID15443640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:33983968..33985706hg38UCSC Ensembl
Innerchr15:34276169..34277907hg19UCSC Ensembl
Innerchr15:32063461..32065199hg18UCSC Ensembl
Innerchr15:32063461..32065199hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381739
hg191739
hg181739
hg171739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657861, nssv658282, nssv654952, nssv689552, nssv689788, nssv667724
Samples
Known GenesAVEN, CHRM5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516347
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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