A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602453



Internal ID6989487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140574364..140582304hg38UCSC Ensembl
Innerchr4:140574364..140582304hg38UCSC Ensembl
Outerchr4:140574230..140582485hg38UCSC Ensembl
chr4:141495518..141503458hg19UCSC Ensembl
Innerchr4:141495518..141503458hg19UCSC Ensembl
Outerchr4:141495384..141503639hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg387941
hg197941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11634703, essv11634702, essv11634701
SamplesHG01571, HG02146, HG01973
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602453
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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