A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192347



Internal ID20759387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:46339021..46449695hg38UCSC Ensembl
chr14:46808224..46918898hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38110675
hg19110675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479582
Supporting Variants
Samples
Known GenesLINC00871
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192347
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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