A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031595



Internal ID18774129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187935080..188218104hg38UCSC Ensembl
Innerchr4:188856234..189139258hg19UCSC Ensembl
Innerchr4:189093228..189376252hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38283025
hg19283025
hg18283025
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636413
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)nsv1031595
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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