A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527474



Internal ID15454767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53582394..53699636hg38UCSC Ensembl
Innerchr15:53874591..53991833hg19UCSC Ensembl
Innerchr15:51661883..51779125hg18UCSC Ensembl
Innerchr15:51661883..51779125hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38117243
hg19117243
hg18117243
hg17117243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703918
Samples
Known GenesWDR72
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527474
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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