A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736794



Internal ID160460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47461787..47461970hg38UCSC Ensembl
chrX:47321186..47321369hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414202
Supporting Variants
Samples
Known GenesZNF41
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736794
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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