A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527161



Internal ID15454454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20911453..20969018hg38UCSC Ensembl
Innerchr17:20814766..20872331hg19UCSC Ensembl
Innerchr17:20755358..20812923hg18UCSC Ensembl
Innerchr17:20755358..20812923hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3857566
hg1957566
hg1857566
hg1757566
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703555
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527161
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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