A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638511



Internal ID21830558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97185451..97185451hg38UCSC Ensembl
chrX:96440450..96440450hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056040
Supporting Variants
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638511
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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