A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602426



Internal ID6989460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:138853277..138865605hg38UCSC Ensembl
Innerchr4:138853293..138865589hg38UCSC Ensembl
Outerchr4:138853261..138865621hg38UCSC Ensembl
chr4:139774431..139786759hg19UCSC Ensembl
Innerchr4:139774447..139786743hg19UCSC Ensembl
Outerchr4:139774415..139786775hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3812329
hg1912329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11632888
SamplesNA18995
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602426
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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