A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601795



Internal ID16389204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31321995..31372298hg38UCSC Ensembl
Innerchr6:31289772..31340075hg19UCSC Ensembl
Innerchr6:31397751..31448054hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3850304
hg1950304
hg1850304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10411n54
Supporting Variantsnssv1053240
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)nsv601795
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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