A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674929



Internal ID18626524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:590949..766894hg38UCSC Ensembl
Innerchr8:540949..716894hg19UCSC Ensembl
Innerchr8:530949..706894hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38175946
hg19175946
hg18175946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032470
Supporting Variants
Samples
Known GenesERICH1, ERICH1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3674929
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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