A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1067379



Internal ID15573879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85405048..85554656hg38UCSC Ensembl
Innerchr6:86114766..86264374hg19UCSC Ensembl
Innerchr6:86171485..86321093hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38149609
hg19149609
hg18149609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604092
Supporting Variants
Samples
Known GenesNT5E, SNX14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1067379
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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