A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11578092



Internal ID6131536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:116695684..116727998hg38UCSC Ensembl
chr4:117616840..117649154hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3832315
hg1932315
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3601903
Supporting Variants
SamplesNA19664
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11578092
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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