A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739476



Internal ID163142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17619311..17620044hg38UCSC Ensembl
chrX:17637431..17638164hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432505
Supporting Variants
Samples
Known GenesNHS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739476
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004527


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