A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11449909



Internal ID4187166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:60915379..60932962hg38UCSC Ensembl
Innerchr4:60915879..60932462hg38UCSC Ensembl
Outerchr4:60914379..60933962hg38UCSC Ensembl
chr4:61781097..61798680hg19UCSC Ensembl
Innerchr4:61781597..61798180hg19UCSC Ensembl
Outerchr4:61780097..61799680hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3817584
hg1917584
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600674
Supporting Variants
SamplesHG03779
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11449909
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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