A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138780



Internal ID337964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141879381..141897381hg38UCSC Ensembl
chrX:140967167..140985167hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3818001
hg1918001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742762
Samples
Known GenesMAGEC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138780
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