A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601899



Internal ID16042622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392612..31482001hg38UCSC Ensembl
Innerchr6:31360389..31449778hg19UCSC Ensembl
Innerchr6:31468368..31557757hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3889390
hg1989390
hg1889390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1053428
Samples
Known GenesHCG26, HCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601899
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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