A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644135



Internal ID21836182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14493663..14493727hg38UCSC Ensembl
chrX:14511785..14511849hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111619
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644135
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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