A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11629996



Internal ID6911031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:137846300..137858516hg38UCSC Ensembl
chr4:138767454..138779670hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3812217
hg1912217
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602405
Supporting Variants
SamplesNA21113
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11629996
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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