A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524065



Internal ID8418340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58433640..58438690hg38UCSC Ensembl
Innerchr15:58725839..58730889hg19UCSC Ensembl
Innerchr15:56513131..56518181hg18UCSC Ensembl
Innerchr15:56513131..56518181hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg385051
hg195051
hg185051
hg175051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699933
Samples
Known GenesLIPC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524065
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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