A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13885908



Internal ID5642339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87516045..87516804hg38UCSC Ensembl
Innerchr10:87516045..87516804hg38UCSC Ensembl
Outerchr10:87516045..87516804hg38UCSC Ensembl
chr10:89275802..89276561hg19UCSC Ensembl
Innerchr10:89275802..89276561hg19UCSC Ensembl
Outerchr10:89275802..89276561hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38760
hg19760
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624110
Supporting Variants
SamplesNA19063
Known GenesMINPP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13885908
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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