A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11395448



Internal ID4228482
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600240
Supporting Variants
SamplesHG03803
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11395448
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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