A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553595



Internal ID16341004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18075934..18078015hg38UCSC Ensembl
Innerchr11:18097481..18099562hg19UCSC Ensembl
Innerchr11:18054057..18056138hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382082
hg192082
hg182082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1668n54
Supporting Variantsnssv768336
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553595
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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