A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555182



Internal ID15995905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64019917..64082340hg38UCSC Ensembl
Innerchr11:63787389..63849812hg19UCSC Ensembl
Innerchr11:63543965..63606388hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3862424
hg1962424
hg1862424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777145
Samples
Known GenesMACROD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555182
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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