A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283671



Internal ID20492889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122033639..122033639hg38UCSC Ensembl
chrX:121167492..121167492hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752961
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283671
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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