A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020359



Internal ID20587399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61421964..61430569hg38UCSC Ensembl
chr14:61888682..61897287hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg388606
hg198606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491470
Supporting Variants
Samples
Known GenesPRKCH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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