A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417653



Internal ID196845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132229387..132229481hg38UCSC Ensembl
chrX:131363415..131363509hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417653
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