A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516536



Internal ID20889897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62759894..62763918hg38UCSC Ensembl
chr18:60427127..60431151hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg384025
hg194025
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18043379
Samples
Known GenesPHLPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516536
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