A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11357237



Internal ID4574580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11846695..11946592hg38UCSC Ensembl
Innerchr4:11846695..11946592hg38UCSC Ensembl
Outerchr4:11846195..11947092hg38UCSC Ensembl
chr4:11848319..11948216hg19UCSC Ensembl
Innerchr4:11848319..11948216hg19UCSC Ensembl
Outerchr4:11847819..11948716hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3899898
hg1999898
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3599659
Supporting Variants
SamplesHG04080
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11357237
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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