A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685519



Internal ID21207377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40192314..40192314hg38UCSC Ensembl
chr3:40233805..40233805hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809444
Supporting Variants
Samples
Known GenesEIF1B-AS1, MYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685519
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.796875


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