A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738413



Internal ID162079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12331388..12562123hg38UCSC Ensembl
chrY:14452115..14674057hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38230736
hg19221943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138238
Supporting Variants
Samples
Known GenesGYG2P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738413
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00314268


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