A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555271



Internal ID15995994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67605006..67666398hg38UCSC Ensembl
Innerchr11:67372477..67433869hg19UCSC Ensembl
Innerchr11:67129053..67190445hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3861393
hg1961393
hg1861393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1982n54
Supporting Variantsnssv1174813
Samples1780862484_A
Known GenesACY3, ALDH3B2, DOC2GP, NDUFV1, NUDT8, TBX10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555271
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