A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466189



Internal ID22524079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20260212..20445457hg38UCSC Ensembl
chrY:22422098..22607343hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38185246
hg19185246
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466189
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