A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644740



Internal ID21836787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109772024..109772024hg38UCSC Ensembl
chrX:109015253..109015253hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053826
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644740
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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