A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023735



Internal ID19112952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170567965..170673434hg38UCSC Ensembl
Innerchr6:170877053..170982522hg19UCSC Ensembl
Innerchr6:170718978..170824447hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38105470
hg19105470
hg18105470
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6209n100
Supporting Variantsnssv3653104, nssv3653103, nssv3653102
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)nsv1023735
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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