A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601822



Internal ID16389231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31340853..31359557hg38UCSC Ensembl
Innerchr6:31308630..31327334hg19UCSC Ensembl
Innerchr6:31416609..31435313hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3818705
hg1918705
hg1818705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10439n54
Supporting Variantsnssv1154247
SamplesHGDP00491
Known GenesHLA-B, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601822
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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