A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2793697



Internal ID21239035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75032864..75032864hg38UCSC Ensembl
chr14:75499567..75499567hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691893
Samples
Known GenesMLH3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2793697
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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