A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618480



Internal ID21566785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:408796..408796hg38UCSC Ensembl
chrY:319531..319531hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171232, nssv17171233
SamplesHG00512, HG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618480
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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