A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426697



Internal ID205623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3020553..3020635hg38UCSC Ensembl
chrY:2888594..2888676hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738270
Samples
Known GenesLINC00278
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426697
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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