A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738258



Internal ID161924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155891000..155903000hg38UCSC Ensembl
chrX:155120663..155132664hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3812001
hg1912002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424054
Supporting Variants
Samples
Known GenesVAMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738258
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00041841


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