A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2813694



Internal ID21259032
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 StatusM
Merged Variants
Supporting Variantsnssv13709727
Samples
Known GenesACOT13
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2813694
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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