A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566521



Internal ID20939592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149171173..149171755hg38UCSC Ensembl
chr3:148888960..148889542hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262580
Samples
Known GenesCP, HPS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566521
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