A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257026



Internal ID21398989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18172892..18292282hg38UCSC Ensembl
chrY:20334778..20454168hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38119391
hg19119391
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730088
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257026
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