A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544897



Internal ID20918135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155107917..155116118hg38UCSC Ensembl
chr1:155080393..155088594hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg388202
hg198202
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247105
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544897
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