A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13715207



Internal ID6019659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21327903..21338106hg38UCSC Ensembl
chr10:21616832..21627035hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3810204
hg1910204
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622576
Supporting Variants
SamplesNA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13715207
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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