A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556432



Internal ID15997155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:108227836..108244812hg38UCSC Ensembl
Innerchr11:108098563..108115539hg19UCSC Ensembl
Innerchr11:107603773..107620749hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3816977
hg1916977
hg1816977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2181n54
Supporting Variantsnssv784565
Samples
Known GenesATM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556432
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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