A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376430



Internal ID22602099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27234964..27235278hg38UCSC Ensembl
chr17:25561990..25562304hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376430
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