A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541248



Internal ID20914529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98496751..98497526hg38UCSC Ensembl
chr2:99113214..99113989hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38776
hg19776
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4067n223
Supporting Variantsnssv18261679
Samples
Known GenesINPP4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541248
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