A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613654



Internal ID16401063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15601973..15638366hg38UCSC Ensembl
Innerchr9:15601971..15638364hg19UCSC Ensembl
Innerchr9:15591971..15628364hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3836394
hg1936394
hg1836394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1128804
Samples
Known GenesCCDC171
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613654
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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