A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521336



Internal ID15101943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70915612..71074673hg38UCSC Ensembl
Innerchr15:71207951..71367012hg19UCSC Ensembl
Innerchr15:68995005..69154066hg18UCSC Ensembl
Innerchr15:68995005..69154066hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38159062
hg19159062
hg18159062
hg17159062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv153n21
Supporting Variantsnssv697944
Samples
Known GenesLRRC49
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521336
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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