A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11359739



Internal ID1219259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14423488..14463871hg38UCSC Ensembl
chr4:14425112..14465495hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3840384
hg1940384
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599723
Supporting Variants
SamplesHG01083
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11359739
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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