A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399114



Internal ID21056667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:141241824..141247458hg38UCSC Ensembl
chr5:140621392..140627026hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg385635
hg195635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125223
Samples
Known GenesPCDHB15, PCDHB19P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399114
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