A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390276



Internal ID21047829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:81132841..81133908hg38UCSC Ensembl
chr4:82053995..82055062hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg381068
hg191068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119809
Samples
Known GenesPRKG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390276
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