A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736491



Internal ID160157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40080064..40080064hg38UCSC Ensembl
chrX:39939317..39939317hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535633
Supporting Variants
Samples
Known GenesBCOR
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736491
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.213354


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