A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018893



Internal ID18761426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:187167070..188502822hg38UCSC Ensembl
Innerchr4:188088224..189423976hg19UCSC Ensembl
Innerchr4:188325218..189660970hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381335753
hg191335753
hg181335753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5496n100
Supporting Variantsnssv3635644
Samples
Known GenesLINC01060, LOC339975, TRIML1, 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)nsv1018893
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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