A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768868



Internal ID16062824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22446051..22451212hg38UCSC Ensembl
Innerchr11:22467597..22472758hg19UCSC Ensembl
Innerchr11:22424173..22429334hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg385162
hg195162
hg185162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553729
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)nssv768868
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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