A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738169



Internal ID161835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155071051..155217414hg38UCSC Ensembl
chrX:154299326..154445691hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38146364
hg19146366
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425627
Supporting Variants
Samples
Known GenesBRCC3, CMC4, MTCP1, VBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738169
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000832466


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