A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139074



Internal ID338258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75668542..75684542hg38UCSC Ensembl
chrX:74888377..74904377hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3816001
hg1916001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139074
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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