A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778993



Internal ID15726263
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 StatusS
Merged Variantsnsv555409
Supporting Variants
Samples
Known GenesARAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778993
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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