A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020082



Internal ID19109301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156350099..156433472hg38UCSC Ensembl
Innerchr6:156671233..156754606hg19UCSC Ensembl
Innerchr6:156712925..156796298hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3883374
hg1983374
hg1883374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654486
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)nsv1020082
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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