A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022128



Internal ID18764662
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 StatusM
Merged Variants
Supporting Variantsnssv3744539
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)nsv1022128
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