A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv785101



Internal ID15732371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130022917..130069931hg38UCSC Ensembl
Innerchr11:129892812..129939826hg19UCSC Ensembl
Innerchr11:129398022..129445036hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3847015
hg1947015
hg1847015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556566
Supporting Variants
Samples
Known GenesAPLP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv785101
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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