A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581706



Internal ID20954777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59627387..59628055hg38UCSC Ensembl
chr10:61387145..61387813hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv760n223
Supporting Variantsnssv18235311
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581706
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