A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555209



Internal ID15995932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64894060..64916816hg38UCSC Ensembl
Innerchr11:64661532..64684288hg19UCSC Ensembl
Innerchr11:64418108..64440864hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3822757
hg1922757
hg1822757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777173
Samples
Known GenesATG2A, MIR6749, MIR6750
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555209
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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