A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5515212



Internal ID291696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22478462..23207673hg38UCSC Ensembl
chr19:22661264..23390475hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38729212
hg19729212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722438
Samples
Known GenesLOC100996349, LOC440518, ZNF492, ZNF728, ZNF730, ZNF99
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5515212
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer