A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555807



Internal ID20928878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172961039..172962277hg38UCSC Ensembl
chr3:172678829..172680067hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg381239
hg191239
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259884
Samples
Known GenesSPATA16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555807
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