A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138168



Internal ID337351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:93016000..93025300hg38UCSC Ensembl
chrX:92270999..92280299hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg389301
hg199301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138168
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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