A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13863617



Internal ID6026088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74139556..74143171hg38UCSC Ensembl
Innerchr10:74139556..74143171hg38UCSC Ensembl
Outerchr10:74139300..74143436hg38UCSC Ensembl
chr10:75899314..75902929hg19UCSC Ensembl
Innerchr10:75899314..75902929hg19UCSC Ensembl
Outerchr10:75899058..75903194hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg383616
hg193616
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623824
Supporting Variants
SamplesNA19435
Known GenesAP3M1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13863617
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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