A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522373



Internal ID8416648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58537336..58544739hg38UCSC Ensembl
Innerchr15:58829535..58836938hg19UCSC Ensembl
Innerchr15:56616827..56624230hg18UCSC Ensembl
Innerchr15:56616827..56624230hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg387404
hg197404
hg187404
hg177404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694160
Samples
Known GenesLIPC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522373
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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