A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683418



Internal ID21205274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16739587..16739587hg38UCSC Ensembl
chr4:16741210..16741210hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809804
Supporting Variants
Samples
Known GenesLDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683418
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.37931


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