A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927666



Internal ID22702896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43477219..43477822hg38UCSC Ensembl
chr19:43981371..43981974hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390085
Samples
Known GenesPHLDB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927666
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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