A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891888



Internal ID19186284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:100392540..100417971hg38UCSC Ensembl
Outerchr10:100392540..100425497hg38UCSC Ensembl
Innerchr10:102152297..102177728hg19UCSC Ensembl
Outerchr10:102152297..102185254hg19UCSC Ensembl
Innerchr10:102142287..102167718hg18UCSC Ensembl
Outerchr10:102142287..102175244hg18UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg3832958
hg1932958
hg1832958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783719, essv25783350
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891888
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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