A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258577



Internal ID21400435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14019675..14049366hg38UCSC Ensembl
chrY:16131555..16161246hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3829692
hg1929692
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730227
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258577
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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