A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525464



Internal ID301623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9658031..9660544hg38UCSC Ensembl
chr19:9768707..9771220hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382514
hg192514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721241
Samples
Known GenesZNF562
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525464
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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