A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648933



Internal ID21840980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20758739..20758828hg38UCSC Ensembl
chrX:20776857..20776946hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106067
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648933
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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