A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556595



Internal ID15997318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133888642..133913337hg38UCSC Ensembl
Innerchr11:133758537..133783232hg19UCSC Ensembl
Innerchr11:133263747..133288442hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3824696
hg1924696
hg1824696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176205
SamplesHGDP00976
Known GenesIGSF9B, MIR4697, MIR4697HG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556595
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer