A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483774



Internal ID21141327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60809654..60875449hg38UCSC Ensembl
chr14:61276372..61342167hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3865796
hg1965796
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020317
Samples
Known GenesMNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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