A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601695



Internal ID16389104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31316476..31354420hg38UCSC Ensembl
Innerchr6:31284253..31322197hg19UCSC Ensembl
Innerchr6:31392232..31430176hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3837945
hg1937945
hg1837945
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10381n54
Supporting Variantsnssv1053064
Samples
Known GenesHLA-B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601695
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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