A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv780814



Internal ID16074770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90801032..90837619hg38UCSC Ensembl
Innerchr11:90534200..90570787hg19UCSC Ensembl
Innerchr11:90173848..90210435hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3836588
hg1936588
hg1836588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555883
Supporting Variants
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv780814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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