A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798874



Internal ID21244212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:6544393..6544393hg38UCSC Ensembl
chr18:6544392..6544392hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13676813
Samples
Known GenesC18orf64
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798874
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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