A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698736



Internal ID21220586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35692288..35692288hg38UCSC Ensembl
chrX:35710405..35710405hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818903
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698736
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.546875


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