A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768948



Internal ID16062904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22998359..23022607hg38UCSC Ensembl
Innerchr11:23019905..23044153hg19UCSC Ensembl
Innerchr11:22976481..23000729hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3824249
hg1924249
hg1824249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553750
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)nssv768948
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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