A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18020117



Internal ID20587157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:62794326..62806283hg38UCSC Ensembl
chr14:63261044..63273001hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3811958
hg1911958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6490735
Supporting Variants
Samples
Known GenesKCNH5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18020117
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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