A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13710452



Internal ID21232222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16266440..16266440hg38UCSC Ensembl
chr6:16266671..16266671hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813791
Supporting Variants
Samples
Known GenesGMPR
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13710452
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.413793


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