A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624834



Internal ID7011684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125409622..125422210hg38UCSC Ensembl
Innerchr10:125409622..125422210hg38UCSC Ensembl
Outerchr10:125409122..125422710hg38UCSC Ensembl
chr10:127098191..127110779hg19UCSC Ensembl
Innerchr10:127098191..127110779hg19UCSC Ensembl
Outerchr10:127097691..127111279hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3812589
hg1912589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13963729
SamplesNA20862
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624834
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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