A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678723



Internal ID21200580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10792060..10792060hg38UCSC Ensembl
chr10:10834023..10834023hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788198
Supporting Variants
Samples
Known GenesSFTA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678723
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.225806


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