A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532560



Internal ID308480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57324349..57325079hg38UCSC Ensembl
chr19:57835717..57836447hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724332
Samples
Known GenesZNF543
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532560
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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