A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490278



Internal ID21147831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27562703..27631195hg38UCSC Ensembl
chr14:28031909..28100401hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3868493
hg1968493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017055
Samples
Known GenesLINC00645
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490278
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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