A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604263



Internal ID16391672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100532998..100630842hg38UCSC Ensembl
Innerchr6:100980874..101078718hg19UCSC Ensembl
Innerchr6:101087595..101185439hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3897845
hg1997845
hg1897845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10862n54
Supporting Variantsnssv1070560
Samples
Known GenesASCC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604263
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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