A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291291



Internal ID20500509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103525123..103525123hg38UCSC Ensembl
chrX:102780051..102780051hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg381731
hg191731
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740476
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291291
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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