A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739411



Internal ID163077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15957820..15958988hg38UCSC Ensembl
chrX:15975943..15977111hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg381169
hg191169
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429869
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739411
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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