A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033733



Internal ID19122954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80931574..81019065hg38UCSC Ensembl
Innerchr6:81641291..81728782hg19UCSC Ensembl
Innerchr6:81698010..81785501hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3887492
hg1987492
hg1887492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648867
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)nsv1033733
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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