A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603737



Internal ID16391146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:73999845..74015647hg38UCSC Ensembl
Innerchr6:74709561..74725363hg19UCSC Ensembl
Innerchr6:74766281..74782083hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3815803
hg1915803
hg1815803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1064427
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603737
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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