A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1066953



Internal ID15920139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78333273..78745565hg38UCSC Ensembl
Innerchr6:79042990..79455282hg19UCSC Ensembl
Innerchr6:79099709..79512001hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38412293
hg19412293
hg18412293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604011
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)nssv1066953
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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