A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601896



Internal ID16042619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31392612..31469528hg38UCSC Ensembl
Innerchr6:31360389..31437305hg19UCSC Ensembl
Innerchr6:31468368..31545284hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3876917
hg1976917
hg1876917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10457n54
Supporting Variantsnssv1053422
Samples
Known GenesHCP5, MICA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601896
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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