A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13701698



Internal ID21223525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115436031..115436031hg38UCSC Ensembl
chrX:114670788..114670788hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13701698
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.8125


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