A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696175



Internal ID21218026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46201374..46201374hg38UCSC Ensembl
chr21:47621288..47621288hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803990
Supporting Variants
Samples
Known GenesLSS
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696175
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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