A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077394



Internal ID15930580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170055797..170079651hg38UCSC Ensembl
Innerchr6:170371021..170394875hg19UCSC Ensembl
Innerchr6:170212946..170236800hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3823855
hg1923855
hg1823855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605531
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)nssv1077394
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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