A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644819



Internal ID21836866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:69261693..69261693hg38UCSC Ensembl
chrX:68481536..68481536hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644819
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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