A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15746837



Internal ID21384941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142201266..142207979hg38UCSC Ensembl
chr5:141580831..141587544hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg386714
hg196714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434517
Supporting Variants
SamplesBTQ038
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15746837
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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