A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593670



Internal ID20966741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45667229..45800836hg38UCSC Ensembl
chr10:46162677..46296284hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38133608
hg19133608
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230336
Samples
Known GenesFAM21C, ZFAND4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593670
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