A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891862



Internal ID18839572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76362971..76486334hg38UCSC Ensembl
Outerchr10:76362971..76486334hg38UCSC Ensembl
Innerchr10:78122729..78246092hg19UCSC Ensembl
Outerchr10:78122729..78246092hg19UCSC Ensembl
Innerchr10:77792735..77916098hg18UCSC Ensembl
Outerchr10:77792735..77916098hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38123364
hg19123364
hg18123364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799663
Samples
Known GenesC10orf11
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891862
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