A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553826



Internal ID16341235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24757415..24781515hg38UCSC Ensembl
Innerchr11:24778961..24803061hg19UCSC Ensembl
Innerchr11:24735537..24759637hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3824101
hg1924101
hg1824101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174761
Samples1780862459_A
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553826
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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