A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017579



Internal ID20584619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:29615993..29623135hg38UCSC Ensembl
chr14:30085199..30092341hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg387143
hg197143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479985
Supporting Variants
Samples
Known GenesMIR548AI, PRKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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