A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019242



Internal ID19108460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102229496..102287407hg38UCSC Ensembl
Innerchr6:102677371..102735282hg19UCSC Ensembl
Innerchr6:102784064..102841975hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3857912
hg1957912
hg1857912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6114n100
Supporting Variantsnssv3649863
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)nsv1019242
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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