A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268896



Internal ID20478114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153126239..153126239hg38UCSC Ensembl
chrX:152392034..152392034hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268896
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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