A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205807



Internal ID21344605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12661152..12661152hg38UCSC Ensembl
chrY:14773083..14773083hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938118
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205807
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