A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13935594



Internal ID5969031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111408963..111425272hg38UCSC Ensembl
chr10:113168721..113185030hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3816310
hg1916310
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624557
Supporting Variants
SamplesNA19379
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13935594
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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