A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696144



Internal ID21217995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2080411..2080411hg38UCSC Ensembl
chr4:2082138..2082138hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809111
Supporting Variants
Samples
Known GenesPOLN
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696144
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.529412


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