A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv780932



Internal ID15728202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92195159..92251289hg38UCSC Ensembl
Innerchr11:91928325..91984455hg19UCSC Ensembl
Innerchr11:91567973..91624103hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3856131
hg1956131
hg1856131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555902
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)nssv780932
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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