A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031608



Internal ID19120830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170555631..170591291hg38UCSC Ensembl
Innerchr6:170864719..170900379hg19UCSC Ensembl
Innerchr6:170706644..170742304hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3835661
hg1935661
hg1835661
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6208n100
Supporting Variantsnssv3653099
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)nsv1031608
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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