A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170516



Internal ID21403861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26652990..26656365hg38UCSC Ensembl
chrY:28799137..28802512hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg383376
hg193376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668697
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170516
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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