A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170882



Internal ID21431617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56829352..56829431hg38UCSC Ensembl
chrY:58975499..58975578hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671053
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170882
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