A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268171



Internal ID20477389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27528008..27528008hg38UCSC Ensembl
chrX:27546125..27546125hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4731714
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268171
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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