A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439894



Internal ID22497764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65923245..66133038hg38UCSC Ensembl
chr6:66633138..66842931hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38209794
hg19209794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971035
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439894
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer