A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763959



Internal ID15711229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1078904..1225711hg38UCSC Ensembl
Innerchr11:1078980..1246941hg19UCSC Ensembl
Innerchr11:1068980..1203517hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38146808
hg19167962
hg18134538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552921
Supporting Variants
Samples
Known GenesMUC2, MUC5B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv763959
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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