A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890727



Internal ID19185029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120851124..120940247hg38UCSC Ensembl
Outerchr5:120847451..120940372hg38UCSC Ensembl
Innerchr5:120186819..120275942hg19UCSC Ensembl
Outerchr5:120183146..120276067hg19UCSC Ensembl
Innerchr5:120214718..120303841hg18UCSC Ensembl
Outerchr5:120211045..120303966hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3892922
hg1992922
hg1892922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781691, essv25782983
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890727
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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