A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524827



Internal ID301018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50365143..50365251hg38UCSC Ensembl
chr19:50868400..50868508hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724096
Samples
Known GenesNAPSA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524827
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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