A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601827



Internal ID16389236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31345562..31372094hg38UCSC Ensembl
Innerchr6:31313339..31339871hg19UCSC Ensembl
Innerchr6:31421318..31447850hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3826533
hg1926533
hg1826533
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10440n54
Supporting Variantsnssv1053303
Samples
Known GenesHLA-B, MIR6891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601827
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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