A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11619926



Internal ID6687820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135521461..135576224hg38UCSC Ensembl
chr4:136442616..136497379hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3854764
hg1954764
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602332
Supporting Variants
SamplesNA20818
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11619926
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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