A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648708



Internal ID21840755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17798214..17798214hg38UCSC Ensembl
chrX:17816334..17816334hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6041875
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648708
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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