A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250537



Internal ID20817577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62248771..62249072hg38UCSC Ensembl
chr1:62714443..62714744hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554133
Supporting Variants
Samples
Known GenesKANK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250537
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer