A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789371



Internal ID19179652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188339654..188741515hg38UCSC Ensembl
Innerchr4:189260808..189662669hg19UCSC Ensembl
Innerchr4:189497802..189899663hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38401862
hg19401862
hg18401862
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894094
Supporting Variants
Samples
Known GenesLINC01060
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=168
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789371
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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