A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481972



Internal ID21139525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86897961..86932779hg38UCSC Ensembl
chr14:87364305..87399123hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3834819
hg1934819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022366
Samples
Known GenesLOC283585
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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