A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13913023



Internal ID3754087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101031682..101032574hg38UCSC Ensembl
Innerchr10:101031732..101032524hg38UCSC Ensembl
Outerchr10:101031626..101032630hg38UCSC Ensembl
chr10:102791439..102792331hg19UCSC Ensembl
Innerchr10:102791489..102792281hg19UCSC Ensembl
Outerchr10:102791383..102792387hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38893
hg19893
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624367
Supporting Variants
SamplesHG03382
Known GenesSFXN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13913023
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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