A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599396



Internal ID6986444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1860368..1860600hg38UCSC Ensembl
Innerchr4:1860367..1860601hg38UCSC Ensembl
Outerchr4:1860368..1860600hg38UCSC Ensembl
chr4:1862095..1862327hg19UCSC Ensembl
Innerchr4:1862328..1862094hg19UCSC Ensembl
Outerchr4:1862095..1862327hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11315988, essv11315986, essv11315987, essv11315989
SamplesNA18867, NA19318, HG01685, NA19467
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599396
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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