A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547764



Internal ID20920965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100341371..100341773hg38UCSC Ensembl
chr3:100060215..100060617hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38403
hg19403
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258866
Samples
Known GenesNIT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547764
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