A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550775



Internal ID20923915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225788226..225788630hg38UCSC Ensembl
chr1:225975928..225976332hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249420
Samples
Known GenesSRP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550775
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