A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529731



Internal ID305742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41326350..41326556hg38UCSC Ensembl
chr19:41832255..41832461hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529731
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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