A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555277



Internal ID15996000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67997585..68027175hg38UCSC Ensembl
Innerchr11:67765056..67794643hg19UCSC Ensembl
Innerchr11:67521632..67551219hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3829591
hg1929588
hg1829588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174816
Samples1780862226_A
Known GenesALDH3B1, UNC93B1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555277
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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