A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138647



Internal ID337831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:93611370..93619858hg38UCSC Ensembl
chrX:92866369..92874857hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg388489
hg198489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741499
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138647
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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