A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709727



Internal ID21231503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24683760..24683760hg38UCSC Ensembl
chr6:24683988..24683988hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2813694
Supporting Variants
Samples
Known GenesACOT13
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709727
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.640625


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