A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624754



Internal ID7011604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121643289..121650099hg38UCSC Ensembl
Innerchr10:121643289..121650099hg38UCSC Ensembl
Outerchr10:121642789..121650599hg38UCSC Ensembl
chr10:123402803..123409613hg19UCSC Ensembl
Innerchr10:123402803..123409613hg19UCSC Ensembl
Outerchr10:123402303..123410113hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386811
hg196811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13953780, essv13953779, essv13953776, essv13953774, essv13953778, essv13953777, essv13953775
SamplesNA19397, NA19332, HG02946, NA19776, NA19449, NA19440, NA19346
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624754
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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