A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13821520



Internal ID3788907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:55819242..55982426hg38UCSC Ensembl
chr10:57579002..57742186hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38163185
hg19163185
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623359
Supporting Variants
SamplesHG03437
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13821520
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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