A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138962



Internal ID338146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1615333..1665977hg38UCSC Ensembl
chrX:1734226..1784870hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3850645
hg1950645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738877
Samples
Known GenesASMT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138962
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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