A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890717



Internal ID19185019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115756017..115784711hg38UCSC Ensembl
Outerchr5:115749506..115784737hg38UCSC Ensembl
Innerchr5:115091714..115120408hg19UCSC Ensembl
Outerchr5:115085203..115120434hg19UCSC Ensembl
Innerchr5:115119613..115148307hg18UCSC Ensembl
Outerchr5:115113102..115148333hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3835232
hg1935232
hg1835232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797911, essv25779416
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890717
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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