A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642526



Internal ID21834573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65824613..65835518hg38UCSC Ensembl
chrX:65044455..65055360hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3810906
hg1910906
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104312
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642526
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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