A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171189



Internal ID21492062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:268193..268577hg38UCSC Ensembl
chrY:134860..135244hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671113
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171189
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