A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599940



Internal ID6986984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24355085..24359419hg38UCSC Ensembl
Innerchr4:24355101..24359404hg38UCSC Ensembl
Outerchr4:24355070..24359435hg38UCSC Ensembl
chr4:24356708..24361042hg19UCSC Ensembl
Innerchr4:24356724..24361027hg19UCSC Ensembl
Outerchr4:24356693..24361058hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg384335
hg194335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11370593, essv11370592
SamplesHG04033, HG03814
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599940
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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