A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542466



Internal ID20915725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47428054..47429305hg38UCSC Ensembl
chr2:47655193..47656444hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381252
hg191252
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258046
Samples
Known GenesMSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542466
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