A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020627



Internal ID18763162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110982539..111302511hg38UCSC Ensembl
Innerchr6:111303742..111623714hg19UCSC Ensembl
Innerchr6:111410435..111730407hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38319973
hg19319973
hg18319973
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654297
Samples
Known GenesGSTM2P1, KIAA1919, REV3L, RPF2, SLC16A10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020627
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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