A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18017274



Internal ID20584314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35246550..35284969hg38UCSC Ensembl
chr14:35715756..35754175hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3838420
hg1938420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490419
Supporting Variants
Samples
Known GenesKIAA0391, PSMA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18017274
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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