A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794725



Internal ID21240063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18507489..18507489hg38UCSC Ensembl
chr16:14982393..14982393hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13685280
Samples
Known GenesNOMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794725
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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