A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739961



Internal ID163627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:33581257..33662677hg38UCSC Ensembl
chrX:33599374..33680794hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3881421
hg1981421
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427073
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739961
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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