A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13890497



Internal ID4678018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88791335..88872446hg38UCSC Ensembl
chr10:90551092..90632203hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3881112
hg1981112
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624140
Supporting Variants
SamplesHG04202
Known GenesANKRD22, LIPM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13890497
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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