A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936710



Internal ID22712068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3789971..3791411hg38UCSC Ensembl
chr19:3789969..3791409hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381441
hg191441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402759
Samples
Known GenesMATK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936710
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