A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520069



Internal ID15447362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76309871..76316840hg38UCSC Ensembl
Innerchr15:76602212..76609181hg19UCSC Ensembl
Innerchr15:74389267..74396236hg18UCSC Ensembl
Innerchr15:74389267..74396236hg17UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg386970
hg196970
hg186970
hg176970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697205
Samples
Known GenesETFA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520069
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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