A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033482



Internal ID19122703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103268809..103314174hg38UCSC Ensembl
Innerchr6:103716684..103762049hg19UCSC Ensembl
Innerchr6:103823377..103868742hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3845366
hg1945366
hg1845366
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6118n100
Supporting Variantsnssv3649881, nssv3649882
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)nsv1033482
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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