A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599957



Internal ID6640219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25144202..25148270hg38UCSC Ensembl
Innerchr4:25144252..25148220hg38UCSC Ensembl
Outerchr4:25144120..25148352hg38UCSC Ensembl
chr4:25145824..25149892hg19UCSC Ensembl
Innerchr4:25145874..25149842hg19UCSC Ensembl
Outerchr4:25145742..25149974hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg384069
hg194069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11370928
SamplesHG02728
Known GenesSEPSECS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599957
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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