A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639645



Internal ID21831692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97185351..97185351hg38UCSC Ensembl
chrX:96440350..96440350hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043301
Supporting Variants
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639645
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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