A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778549



Internal ID16072505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67028909..67053257hg38UCSC Ensembl
Innerchr11:66796380..66820728hg19UCSC Ensembl
Innerchr11:66552956..66577304hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3824349
hg1924349
hg1824349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555240
Supporting Variants
Samples
Known GenesMIR6860, SYT12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778549
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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