A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556839



Internal ID16344248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:135007772..135070522hg38UCSC Ensembl
Innerchr11:134877666..134940416hg19UCSC Ensembl
Innerchr11:134382876..134445626hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3862751
hg1962751
hg1862751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2239n54
Supporting Variantsnssv785820, nssv785819
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556839
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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