A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559998



Internal ID20933069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99405031..99405194hg38UCSC Ensembl
chr6:99852907..99853070hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272826
Samples
Known GenesPNISR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559998
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