A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687548



Internal ID21209403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51019964..51019964hg38UCSC Ensembl
chr16:51053875..51053875hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795916
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687548
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.965517


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