A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577844



Internal ID20950915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130533040..130544029hg38UCSC Ensembl
chr10:132331304..132342293hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3810990
hg1910990
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577844
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