A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138519



Internal ID337703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154549303..154556100hg38UCSC Ensembl
chrX:153777518..153784315hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386798
hg196798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738131
Samples
Known GenesIKBKG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138519
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