A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5526664



Internal ID302785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55355734..55357781hg38UCSC Ensembl
chr19:55867102..55869149hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725663
Samples
Known GenesFAM71E2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5526664
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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