A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894118



Internal ID19185187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6682887..6699111hg38UCSC Ensembl
Outerchr5:6682887..6699111hg38UCSC Ensembl
Innerchr5:6683000..6699224hg19UCSC Ensembl
Outerchr5:6683000..6699224hg19UCSC Ensembl
Innerchr5:6736000..6752224hg18UCSC Ensembl
Outerchr5:6736000..6752224hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3816225
hg1916225
hg1816225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25784709
Samples
Known GenesLOC100505625
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894118
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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