A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698366



Internal ID21220217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39176862..39176862hg38UCSC Ensembl
chrX:39036115..39036115hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820712
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698366
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.21875


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