A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11438314



Internal ID3106132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53726161..53737177hg38UCSC Ensembl
chr4:54592328..54603344hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3811017
hg1911017
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600532
Supporting Variants
SamplesHG02727
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11438314
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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