A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153692



Internal ID15534442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42085013..42130449hg38UCSC Ensembl
Innerchr6:42052751..42098187hg19UCSC Ensembl
Innerchr6:42160729..42206165hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3845437
hg1945437
hg1845437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602990
Supporting Variants
SamplesNINDS_70
Known GenesC6orf132
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153692
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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