A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479033



Internal ID21136586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:33184193..33209303hg38UCSC Ensembl
chr14:33653399..33678509hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3825111
hg1925111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017879
Samples
Known GenesNPAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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