A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16058882



Internal ID2447455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43044130..43105414hg38UCSC Ensembl
chr19:43548282..43609566hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3861285
hg1961285
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644440
Supporting Variants
SamplesHG02153
Known GenesPSG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16058882
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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