A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547626



Internal ID20920827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235052919..235058426hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385508
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv558n223
Supporting Variantsnssv18250679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547626
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