A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452304



Internal ID22510177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97535101..97535101hg38UCSC Ensembl
chrX:96790100..96790100hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5959964
Supporting Variants
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452304
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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