A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600623



Internal ID6987665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:58274786..58284461hg38UCSC Ensembl
Innerchr4:58274797..58284451hg38UCSC Ensembl
Outerchr4:58274776..58284472hg38UCSC Ensembl
chr4:59140952..59150627hg19UCSC Ensembl
Innerchr4:59140963..59150617hg19UCSC Ensembl
Outerchr4:59140942..59150638hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg389676
hg199676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11444889
SamplesHG01578
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600623
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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