A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890712



Internal ID19185014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113986227..114033908hg38UCSC Ensembl
Outerchr5:113986227..114033908hg38UCSC Ensembl
Innerchr5:113321924..113369605hg19UCSC Ensembl
Outerchr5:113321924..113369605hg19UCSC Ensembl
Innerchr5:113349823..113397504hg18UCSC Ensembl
Outerchr5:113349823..113397504hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3847682
hg1947682
hg1847682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799453
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890712
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer