A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623861



Internal ID6664028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76201978..76206142hg38UCSC Ensembl
Innerchr10:76201978..76206142hg38UCSC Ensembl
Outerchr10:76201867..76206174hg38UCSC Ensembl
chr10:77961736..77965900hg19UCSC Ensembl
Innerchr10:77961736..77965900hg19UCSC Ensembl
Outerchr10:77961625..77965932hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg384165
hg194165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv150e214
Supporting Variantsessv13864477
SamplesHG02009
Known GenesC10orf11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623861
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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