A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11653087



Internal ID1654903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150652515..150654820hg38UCSC Ensembl
Innerchr4:150652540..150654796hg38UCSC Ensembl
Outerchr4:150652491..150654845hg38UCSC Ensembl
chr4:151573667..151575972hg19UCSC Ensembl
Innerchr4:151573692..151575948hg19UCSC Ensembl
Outerchr4:151573643..151575997hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382306
hg192306
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602659
Supporting Variants
SamplesHG04106
Known GenesLRBA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11653087
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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