A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943447



Internal ID21363516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2891928..2891928hg38UCSC Ensembl
chrY:2759969..2759969hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205790
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943447
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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