A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13960024



Internal ID529199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123204963..123237153hg38UCSC Ensembl
Innerchr10:123205463..123236653hg38UCSC Ensembl
Outerchr10:123203963..123238153hg38UCSC Ensembl
chr10:124964479..124996669hg19UCSC Ensembl
Innerchr10:124964979..124996169hg19UCSC Ensembl
Outerchr10:124963479..124997669hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3832191
hg1932191
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624793
Supporting Variants
SamplesHG00231
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13960024
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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