A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636418



Internal ID18934699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188015795..188872654hg38UCSC Ensembl
Innerchr4:188936949..189793808hg19UCSC Ensembl
Innerchr4:189173943..190030802hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38856860
hg19856860
hg18856860
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020663
Supporting Variants
Samples
Known GenesLINC01060, TRIML1, TRIML2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636418
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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