A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575881



Internal ID16363290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:65968396..66137608hg38UCSC Ensembl
Innerchr17:63964514..64133726hg19UCSC Ensembl
Innerchr17:61394976..61564188hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38169213
hg19169213
hg18169213
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5747n54
Supporting Variantsnssv875827
Samples
Known GenesCEP112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575881
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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