A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv781993



Internal ID16075949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:100623264..100643182hg38UCSC Ensembl
Innerchr11:100493995..100513913hg19UCSC Ensembl
Innerchr11:99999205..100019123hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3819919
hg1919919
hg1819919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556128
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)nssv781993
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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