A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13935582



Internal ID6817365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111235239..111253929hg38UCSC Ensembl
chr10:112994997..113013687hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3818691
hg1918691
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624553
Supporting Variants
SamplesNA20897
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13935582
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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