A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913909



Internal ID22689125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31635859..31636156hg38UCSC Ensembl
chr12:31788793..31789090hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913909
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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