A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602558



Internal ID6989591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145299656..145300356hg38UCSC Ensembl
Innerchr4:145299706..145300306hg38UCSC Ensembl
Outerchr4:145299606..145300406hg38UCSC Ensembl
chr4:146220808..146221508hg19UCSC Ensembl
Innerchr4:146220858..146221458hg19UCSC Ensembl
Outerchr4:146220758..146221558hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11641082, essv11641079, essv11641080, essv11641081
SamplesNA19314, HG02895, HG02816, HG03538
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602558
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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