A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293305



Internal ID20502523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154519846..154519846hg38UCSC Ensembl
chrX:153748068..153748068hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750950
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293305
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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