A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599599



Internal ID20972670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19761527..19762203hg38UCSC Ensembl
chr19:19872336..19873012hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247636
Samples
Known GenesLINC00663
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599599
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