A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556529



Internal ID15997252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:126204297..126264724hg38UCSC Ensembl
Innerchr11:126074192..126134619hg19UCSC Ensembl
Innerchr11:125579402..125639829hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3860428
hg1960428
hg1860428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784709
Samples
Known GenesFAM118B, RPUSD4, SRPR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556529
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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