A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601879



Internal ID16042602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31387541..31486588hg38UCSC Ensembl
Innerchr6:31355318..31454365hg19UCSC Ensembl
Innerchr6:31463297..31562344hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3899048
hg1999048
hg1899048
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10453n54
Supporting Variantsnssv1053401
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)nsv601879
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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