A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524049



Internal ID8418324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73320492..73387960hg38UCSC Ensembl
Innerchr15:73612833..73680301hg19UCSC Ensembl
Innerchr15:71399886..71467354hg18UCSC Ensembl
Innerchr15:71399886..71467354hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3867469
hg1967469
hg1867469
hg1767469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699913
Samples
Known GenesHCN4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524049
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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