A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696469



Internal ID21218324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2548774..2548774hg38UCSC Ensembl
chr19:2548772..2548772hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2799586
Supporting Variants
Samples
Known GenesGNG7
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696469
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.125


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