A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1067381



Internal ID15920567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85867136..85939987hg38UCSC Ensembl
Innerchr6:86576854..86649705hg19UCSC Ensembl
Innerchr6:86633573..86706424hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3872852
hg1972852
hg1872852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604096
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1067381
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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