A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706382



Internal ID21228178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123550738..123550738hg38UCSC Ensembl
chrX:122684589..122684589hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820189
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706382
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0555556


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