A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138953



Internal ID338137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:28473488..28525488hg38UCSC Ensembl
chrX:28491605..28543605hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3852001
hg1952001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736330
Samples
Known GenesMIR6134
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138953
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