A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138705



Internal ID337889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109109985..109114193hg38UCSC Ensembl
chrX:108353215..108357423hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg384209
hg194209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741915
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138705
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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