A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553825



Internal ID16341234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24757415..24771614hg38UCSC Ensembl
Innerchr11:24778961..24793160hg19UCSC Ensembl
Innerchr11:24735537..24749736hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3814200
hg1914200
hg1814200
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv769101, nssv769102, nssv1174760
SamplesHGDP00946
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553825
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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