A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606558



Internal ID21554863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:408749..408749hg38UCSC Ensembl
chrY:319484..319484hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171231
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606558
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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