A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577531



Internal ID20950602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27173463..27174312hg38UCSC Ensembl
chr10:27462392..27463241hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222581
Samples
Known GenesMASTL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577531
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