A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760477



Internal ID19058758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19777462..19800506hg38UCSC Ensembl
Innerchr8:19634973..19658017hg19UCSC Ensembl
Innerchr8:19679253..19702297hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3823045
hg1923045
hg1823045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032405
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3760477
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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