A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546461



Internal ID20919680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53919973..53920977hg38UCSC Ensembl
chr1:54385646..54386650hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249786
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546461
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