A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555715



Internal ID16343124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87596661..87638515hg38UCSC Ensembl
Innerchr11:87307553..87349407hg19UCSC Ensembl
Innerchr11:86985201..87027055hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3841855
hg1941855
hg1841855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176193
SamplesHGDP01235
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555715
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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