A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894095



Internal ID18838263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188669388..189430689hg38UCSC Ensembl
Outerchr4:188284250..189545969hg38UCSC Ensembl
Innerchr4:189590542..190351843hg19UCSC Ensembl
Outerchr4:189205404..190467123hg19UCSC Ensembl
Innerchr4:189827536..190588837hg18UCSC Ensembl
Outerchr4:189442398..190704117hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381261720
hg191261720
hg181261720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783143, essv25785593
Samples
Known GenesLINC01060
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894095
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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