A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427811



Internal ID206705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136379124..136385598hg38UCSC Ensembl
chrX:135461283..135467757hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg386475
hg196475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742542
Samples
Known GenesGPR112
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427811
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