A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575882



Internal ID16363291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66004510..66137608hg38UCSC Ensembl
Innerchr17:64000628..64133726hg19UCSC Ensembl
Innerchr17:61431090..61564188hg18UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg38133099
hg19133099
hg18133099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875828
Samples
Known GenesCEP112
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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