A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386587



Internal ID22444457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68804248..68804375hg38UCSC Ensembl
chr17:66800389..66800516hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974178
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386587
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