A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138577



Internal ID337761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:91009024..91158591hg38UCSC Ensembl
chrX:90264023..90413590hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38149568
hg19149568
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138577
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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