A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609472



Internal ID16396881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:665117..977722hg38UCSC Ensembl
Innerchr8:615117..927722hg19UCSC Ensembl
Innerchr8:605117..917722hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38312606
hg19312606
hg18312606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1103535
Samples
Known GenesERICH1, ERICH1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609472
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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