A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521930



Internal ID15449223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:95290849..95299648hg38UCSC Ensembl
Innerchr15:95834078..95842877hg19UCSC Ensembl
Innerchr15:93635082..93643881hg18UCSC Ensembl
Innerchr15:93635082..93643881hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg388800
hg198800
hg188800
hg178800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694699
Samples
Known GenesLOC400456
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521930
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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