A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294105



Internal ID20503323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130466451..130466451hg38UCSC Ensembl
chrX:129600425..129600425hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg382054
hg192054
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294105
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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