A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891754



Internal ID18839464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9363411..9600559hg38UCSC Ensembl
Outerchr10:9363411..9600559hg38UCSC Ensembl
Innerchr10:9405374..9642522hg19UCSC Ensembl
Outerchr10:9405374..9642522hg19UCSC Ensembl
Innerchr10:9445380..9682528hg18UCSC Ensembl
Outerchr10:9445380..9682528hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38237149
hg19237149
hg18237149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782338
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891754
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