A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv782098



Internal ID16076054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103118477..103185951hg38UCSC Ensembl
Innerchr11:102989206..103056680hg19UCSC Ensembl
Innerchr11:102494416..102561890hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3867475
hg1967475
hg1867475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556168
Supporting Variants
Samples
Known GenesDYNC2H1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv782098
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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