A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477977



Internal ID21135530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57593771..57594399hg38UCSC Ensembl
chr14:58060489..58061117hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019838
Samples
Known GenesSLC35F4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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