A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139038



Internal ID338222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:90962542..91070542hg38UCSC Ensembl
chrX:90217541..90325541hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38108001
hg19108001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741410
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139038
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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