A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483611



Internal ID21141164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64057735..64060159hg38UCSC Ensembl
chr14:64524453..64526877hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg382425
hg192425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020668
Samples
Known GenesMIR548AZ, SYNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483611
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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