A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138548



Internal ID337732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155965606..156029606hg38UCSC Ensembl
chrX:155195271..155259271hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3864001
hg1964001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738264
Samples
Known GenesIL9R
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138548
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