A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138367



Internal ID337551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51618000..51676964hg38UCSC Ensembl
chrX:51360852..51419897hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3858965
hg1959046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138367
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