A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674931



Internal ID18626526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:590949..770491hg38UCSC Ensembl
Innerchr8:540949..720491hg19UCSC Ensembl
Innerchr8:530949..710491hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38179543
hg19179543
hg18179543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029208
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)nssv3674931
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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