A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556571



Internal ID15997294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130217050..130289980hg38UCSC Ensembl
Innerchr11:130086945..130159875hg19UCSC Ensembl
Innerchr11:129592155..129665085hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3872931
hg1972931
hg1872931
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176202
Samples1780862229_A
Known GenesZBTB44
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556571
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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