A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574059



Internal ID16014782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:407766..733582hg38UCSC Ensembl
Innerchr17:257557..636822hg19UCSC Ensembl
Innerchr17:257873..583572hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38325817
hg19379266
hg18325700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5386n54
Supporting Variantsnssv864997
Samples
Known GenesC17orf97, FAM101B, FAM57A, VPS53
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574059
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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