A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644362



Internal ID21836409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68239217..68239217hg38UCSC Ensembl
chrX:67459059..67459059hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051704
Supporting Variants
Samples
Known GenesOPHN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644362
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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