A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174760



Internal ID15877180
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 loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553825
Supporting Variants
SamplesHGDP00946
Known GenesLUZP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174760
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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