A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517079



Internal ID22575042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15721247..15736987hg38UCSC Ensembl
chrY:17833127..17848867hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3815741
hg1915741
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968992
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517079
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