A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610867



Internal ID16051590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:27607002..27757379hg38UCSC Ensembl
Innerchr8:27464519..27614896hg19UCSC Ensembl
Innerchr8:27520436..27670815hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38150378
hg19150378
hg18150380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1109356
Samples
Known GenesCCDC25, CLU, MIR3622A, MIR3622B, MIR6843, SCARA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610867
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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