A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11589381



Internal ID2250261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121413073..121474482hg38UCSC Ensembl
Innerchr4:121413083..121474473hg38UCSC Ensembl
Outerchr4:121413064..121474492hg38UCSC Ensembl
chr4:122334228..122395637hg19UCSC Ensembl
Innerchr4:122334238..122395628hg19UCSC Ensembl
Outerchr4:122334219..122395647hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3861410
hg1961410
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602008
Supporting Variants
SamplesHG02014
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11589381
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer