A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13935584



Internal ID6817369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111239334..111254388hg38UCSC Ensembl
Innerchr10:111239484..111254238hg38UCSC Ensembl
Outerchr10:111239184..111254538hg38UCSC Ensembl
chr10:112999092..113014146hg19UCSC Ensembl
Innerchr10:112999242..113013996hg19UCSC Ensembl
Outerchr10:112998942..113014296hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3815055
hg1915055
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624555
Supporting Variants
SamplesNA20897
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13935584
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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