A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13899005



Internal ID859558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92400083..92409576hg38UCSC Ensembl
Innerchr10:92400233..92409426hg38UCSC Ensembl
Outerchr10:92399933..92409726hg38UCSC Ensembl
chr10:94159840..94169333hg19UCSC Ensembl
Innerchr10:94159990..94169183hg19UCSC Ensembl
Outerchr10:94159690..94169483hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg389494
hg199494
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624223
Supporting Variants
SamplesHG00449
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13899005
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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