A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556458



Internal ID15997181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117425576..117471747hg38UCSC Ensembl
Innerchr11:117296292..117342462hg19UCSC Ensembl
Innerchr11:116801502..116847672hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3846172
hg1946171
hg1846171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784605
Samples
Known GenesDSCAML1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556458
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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