A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555096



Internal ID20928185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52924245..52924437hg38UCSC Ensembl
chr1:53389917..53390109hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555096
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