A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600240



Internal ID6987284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37226011..37240019hg38UCSC Ensembl
Innerchr4:37226033..37239998hg38UCSC Ensembl
Outerchr4:37225990..37240041hg38UCSC Ensembl
chr4:37227633..37241641hg19UCSC Ensembl
Innerchr4:37227655..37241620hg19UCSC Ensembl
Outerchr4:37227612..37241663hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3814009
hg1914009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11395448
SamplesHG03803
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600240
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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