A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689977



Internal ID21211834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:44544840..44544840hg38UCSC Ensembl
chr18:42124805..42124805hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2798453
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689977
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.7


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