A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5607046



Internal ID21555351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:323575..323575hg38UCSC Ensembl
chrY:234310..234310hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3815103
hg1915103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170676
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5607046
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