A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644418



Internal ID21836465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155638293..155638351hg38UCSC Ensembl
chrX:154867954..154868012hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107828
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644418
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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