A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526185



Internal ID15453478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64522094..64641783hg38UCSC Ensembl
Innerchr15:64814293..64933982hg19UCSC Ensembl
Innerchr15:62601346..62721035hg18UCSC Ensembl
Innerchr15:62601346..62721035hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38119690
hg19119690
hg18119690
hg17119690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702447
Samples
Known GenesZNF609
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526185
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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