A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138832



Internal ID338016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:88318542..88339000hg38UCSC Ensembl
chrX:87573543..87594001hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3820459
hg1920459
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741305
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138832
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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