A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3744539



Internal ID18696134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187957299..188139456hg38UCSC Ensembl
Innerchr4:188878453..189060610hg19UCSC Ensembl
Innerchr4:189115447..189297604hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38182158
hg19182158
hg18182158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022128
Supporting Variants
Samples
Known GenesTRIML1, TRIML2, ZFP42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3744539
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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