A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738073



Internal ID161739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153405987..153405987hg38UCSC Ensembl
chrX:152671445..152671445hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738073
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000748877


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