A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517404



Internal ID22575368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6488390..6499182hg38UCSC Ensembl
chrY:6356431..6367223hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3810793
hg1910793
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517404
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