A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654392



Internal ID18605987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:131097392..131131160hg38UCSC Ensembl
Innerchr6:131418532..131452300hg19UCSC Ensembl
Innerchr6:131460225..131493993hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3833769
hg1933769
hg1833769
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016925
Supporting Variants
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)nssv3654392
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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