A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687821



Internal ID21209674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46155804..46155804hg38UCSC Ensembl
chr12:46549587..46549587hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791281
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687821
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.984375


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