A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599720



Internal ID6986765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14341174..14348582hg38UCSC Ensembl
Innerchr4:14341174..14348582hg38UCSC Ensembl
Outerchr4:14340939..14348796hg38UCSC Ensembl
chr4:14342798..14350206hg19UCSC Ensembl
Innerchr4:14342798..14350206hg19UCSC Ensembl
Outerchr4:14342563..14350420hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg387409
hg197409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11359726, essv11359725
SamplesNA19922, HG03109
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599720
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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