A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493057



Internal ID21150610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29913021..29921772hg38UCSC Ensembl
chr14:30382227..30390978hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg388752
hg198752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017604
Samples
Known GenesPRKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493057
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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