A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738312



Internal ID161978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7149956..7150058hg38UCSC Ensembl
chrY:7017997..7018099hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738312
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000623


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