A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021812



Internal ID19111030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76879502..77082368hg38UCSC Ensembl
Innerchr6:77589219..77792085hg19UCSC Ensembl
Innerchr6:77645938..77848804hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38202867
hg19202867
hg18202867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6022n100
Supporting Variantsnssv3659051, nssv3659050
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)nsv1021812
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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