A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410377



Internal ID21067930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122432946..122435291hg38UCSC Ensembl
chr5:121768641..121770986hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg382346
hg192346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125528
Samples
Known GenesSNCAIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410377
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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