A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643276



Internal ID21835323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35843710..35873554hg38UCSC Ensembl
chrX:35861827..35891671hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3829845
hg1929845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105049
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643276
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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