A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016982



Internal ID20584022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:27070577..27174241hg38UCSC Ensembl
chr14:27539783..27643447hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38103665
hg19103665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492808
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016982
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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