A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170707



Internal ID21505001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:450560..450714hg38UCSC Ensembl
chrY:361295..361449hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665363
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170707
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