A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432639



Internal ID211377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13668309..13672195hg38UCSC Ensembl
chr1:13994804..13998690hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg383887
hg193887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16895309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432639
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