A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529352



Internal ID305375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13187961..13200581hg38UCSC Ensembl
chr19:13298775..13311395hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812621
hg1912621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv240n206
Supporting Variantsnssv17721568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529352
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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