A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601940



Internal ID16042663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31496186..31513328hg38UCSC Ensembl
Innerchr6:31463963..31481105hg19UCSC Ensembl
Innerchr6:31571942..31589084hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3817143
hg1917143
hg1817143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154292
SamplesNINDS_266
Known GenesMICB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601940
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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