A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604780



Internal ID16392189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140804943..141419781hg38UCSC Ensembl
Innerchr6:141126080..141740918hg19UCSC Ensembl
Innerchr6:141167773..141782611hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38614839
hg19614839
hg18614839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1073822
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604780
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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