A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736682



Internal ID160348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44752478..44754497hg38UCSC Ensembl
chrX:44611724..44613743hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg382020
hg192020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417563
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736682
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001251


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