A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556457



Internal ID15997180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117188631..117257555hg38UCSC Ensembl
Innerchr11:117059347..117128271hg19UCSC Ensembl
Innerchr11:116564557..116633481hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3868925
hg1968925
hg1868925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2186n54
Supporting Variantsnssv784603, nssv784602, nssv784604
Samples
Known GenesLOC100652768, PCSK7, RNF214, SIDT2, TAGLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556457
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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