A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768337



Internal ID16062293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18075934..18078216hg38UCSC Ensembl
Innerchr11:18097481..18099763hg19UCSC Ensembl
Innerchr11:18054057..18056339hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382283
hg192283
hg182283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553596
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)nssv768337
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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