A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640151



Internal ID21832198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57890280..58169396hg38UCSC Ensembl
chrX:57916714..58195830hg19UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg38279117
hg19279117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108913
Supporting Variants
Samples
Known GenesZXDA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640151
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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