A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153431



Internal ID15527814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1181073..1261142hg38UCSC Ensembl
Innerchr4:1174861..1254930hg19UCSC Ensembl
Innerchr4:1164861..1244930hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3880070
hg1980070
hg1880070
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593279
Supporting Variants
SamplesHGDP00546
Known GenesCTBP1, CTBP1-AS, CTBP1-AS2, LOC100130872, SPON2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153431
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