A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv774219



Internal ID16068175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54726769..54771612hg38UCSC Ensembl
Innerchr11:51347668..51392511hg19UCSC Ensembl
Innerchr11:51204244..51249087hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3844844
hg1944844
hg1844844
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554485
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)nssv774219
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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