A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522673



Internal ID15449966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82896959..82901362hg38UCSC Ensembl
Innerchr15:83565711..83570114hg19UCSC Ensembl
Innerchr15:81356715..81361118hg18UCSC Ensembl
Innerchr15:81356715..81361118hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg384404
hg194404
hg184404
hg174404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706078
Samples
Known GenesHOMER2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522673
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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