A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13963729



Internal ID6743608
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624834
Supporting Variants
SamplesNA20862
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13963729
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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