A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1073596



Internal ID15926782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:138381485..138396185hg38UCSC Ensembl
Innerchr6:138702622..138717322hg19UCSC Ensembl
Innerchr6:138744315..138759015hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3814701
hg1914701
hg1814701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604738
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)nssv1073596
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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