A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609452



Internal ID16050175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:240568..919170hg38UCSC Ensembl
Innerchr8:190568..869170hg19UCSC Ensembl
Innerchr8:180568..859170hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38678603
hg19678603
hg18678603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1102102
Samples
Known GenesERICH1, ERICH1-AS1, FAM87A, FBXO25, TDRP, ZNF596
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609452
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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