A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17851761



Internal ID22035404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21212065..21212065hg38UCSC Ensembl
chrY:23373951..23373951hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6243100
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17851761
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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