A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1068419



Internal ID15574919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93771444..93872767hg38UCSC Ensembl
Innerchr6:94481162..94582485hg19UCSC Ensembl
Innerchr6:94537883..94639206hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38101324
hg19101324
hg18101324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604164
Supporting Variants
Samples
Known GenesTSG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1068419
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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