A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138178



Internal ID337361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53902900..53912000hg38UCSC Ensembl
chrX:53929320..53938430hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg389101
hg199111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740130
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138178
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