A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749721



Internal ID19048002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170556081..170591291hg38UCSC Ensembl
Innerchr6:170865169..170900379hg19UCSC Ensembl
Innerchr6:170707094..170742304hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3835211
hg1935211
hg1835211
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025691
Supporting Variants
Samples
Known GenesPDCD2, TBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3749721
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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