A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540428



Internal ID20913720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:55662630..55662922hg38UCSC Ensembl
chr2:55889765..55890057hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258253
Samples
Known GenesPNPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540428
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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