A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688290



Internal ID21210143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168725225..168725225hg38UCSC Ensembl
chr1:168694463..168694463hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2800913
Supporting Variants
Samples
Known GenesDPT
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688290
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.578125


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