A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601936



Internal ID16042659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31471286..31478132hg38UCSC Ensembl
Innerchr6:31439063..31445909hg19UCSC Ensembl
Innerchr6:31547042..31553888hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg386847
hg196847
hg186847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053518
Samples
Known GenesHCG26
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601936
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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