A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555176



Internal ID16342585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63080046..63124412hg38UCSC Ensembl
Innerchr11:62847518..62891884hg19UCSC Ensembl
Innerchr11:62604094..62648460hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3844367
hg1944367
hg1844367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174806
SamplesNINDS_36
Known GenesSLC22A24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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