A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495256



Internal ID21152809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:30548649..30570508hg38UCSC Ensembl
chr14:31017855..31039714hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3821860
hg1921860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177874
Samples
Known GenesG2E3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495256
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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