A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894162



Internal ID19185231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29144865..30125340hg38UCSC Ensembl
Outerchr5:29143096..30125340hg38UCSC Ensembl
Innerchr5:29144972..30125447hg19UCSC Ensembl
Outerchr5:29143203..30125447hg19UCSC Ensembl
Innerchr5:29180729..30161204hg18UCSC Ensembl
Outerchr5:29178960..30161204hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38982245
hg19982245
hg18982245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791939, essv25791395, essv25789019
Samples
Known GenesLOC101929681
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894162
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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