A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601328



Internal ID6988366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89878732..89882859hg38UCSC Ensembl
Innerchr4:89878732..89882859hg38UCSC Ensembl
Outerchr4:89878559..89883025hg38UCSC Ensembl
chr4:90799883..90804010hg19UCSC Ensembl
Innerchr4:90799883..90804010hg19UCSC Ensembl
Outerchr4:90799710..90804176hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg384128
hg194128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11530361, essv11530360
SamplesHG01356, HG01148
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601328
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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