A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646848



Internal ID21838895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20644285..20644285hg38UCSC Ensembl
chrX:20662403..20662403hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047740
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646848
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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