A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741410



Internal ID165076
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 StatusS
Merged Variantsnsv6139038
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741410
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000209424


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