A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13933416



Internal ID4331797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110144004..110146437hg38UCSC Ensembl
Innerchr10:110144022..110146420hg38UCSC Ensembl
Outerchr10:110143987..110146455hg38UCSC Ensembl
chr10:111903762..111906195hg19UCSC Ensembl
Innerchr10:111903780..111906178hg19UCSC Ensembl
Outerchr10:111903745..111906213hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg382434
hg192434
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624533
Supporting Variants
SamplesHG03873
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13933416
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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