A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602008



Internal ID6989042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121413073..121474482hg38UCSC Ensembl
Innerchr4:121413083..121474473hg38UCSC Ensembl
Outerchr4:121413064..121474492hg38UCSC Ensembl
chr4:122334228..122395637hg19UCSC Ensembl
Innerchr4:122334238..122395628hg19UCSC Ensembl
Outerchr4:122334219..122395647hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3861410
hg1961410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11589381
SamplesHG02014
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602008
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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