A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13941338



Internal ID1061514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114791716..114801516hg38UCSC Ensembl
Innerchr10:114791716..114801516hg38UCSC Ensembl
Outerchr10:114791216..114802016hg38UCSC Ensembl
chr10:116551475..116561275hg19UCSC Ensembl
Innerchr10:116551475..116561275hg19UCSC Ensembl
Outerchr10:116550975..116561775hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg389801
hg199801
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624620
Supporting Variants
SamplesHG00684
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13941338
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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