A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689899



Internal ID21211753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32031878..32031878hg38UCSC Ensembl
chr10:32320806..32320806hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789647
Supporting Variants
Samples
Known GenesKIF5B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689899
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.596774


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