A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555409



Internal ID15996132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72694405..72712340hg38UCSC Ensembl
Innerchr11:72405450..72423385hg19UCSC Ensembl
Innerchr11:72083098..72101033hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3817936
hg1917936
hg1817936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv778993
Samples
Known GenesARAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555409
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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