A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17647877



Internal ID21839924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112709927..112709927hg38UCSC Ensembl
chrX:111953155..111953155hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38845
hg19845
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6049668
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17647877
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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