A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13883958



Internal ID6633249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86534152..86536994hg38UCSC Ensembl
Innerchr10:86534156..86536990hg38UCSC Ensembl
Outerchr10:86534148..86536998hg38UCSC Ensembl
chr10:88293909..88296751hg19UCSC Ensembl
Innerchr10:88293913..88296747hg19UCSC Ensembl
Outerchr10:88293905..88296755hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg382843
hg192843
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624092
Supporting Variants
SamplesNA20795
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13883958
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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