A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138615



Internal ID337799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135247381..135253381hg38UCSC Ensembl
chrX:134381328..134387329hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg386001
hg196002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138615
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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