A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689928



Internal ID21211783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12810912..12810912hg38UCSC Ensembl
chr4:49168251..49168251hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689928
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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