A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642551



Internal ID21834598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119208353..119208353hg38UCSC Ensembl
chrX:118342316..118342316hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642551
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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