A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739063



Internal ID162729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6417488..6533800hg38UCSC Ensembl
chrX:6335529..6451841hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38116313
hg19116313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138061
Supporting Variants
Samples
Known GenesVCX3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739063
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000209161


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