A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13431911



Internal ID928764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24082372..24142769hg38UCSC Ensembl
chr9:24082370..24142767hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3860398
hg1960398
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620025
Supporting Variants
SamplesHG00554
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13431911
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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