A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556575



Internal ID16343984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130906629..131144852hg38UCSC Ensembl
Innerchr11:130776524..131014747hg19UCSC Ensembl
Innerchr11:130281734..130519957hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38238224
hg19238224
hg18238224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785111, nssv785112
Samples
Known GenesSNX19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556575
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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