A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488464



Internal ID21146017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60910771..60938687hg38UCSC Ensembl
chr14:61377489..61405405hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3827917
hg1927917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020331
Samples
Known GenesMNAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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