A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194121



Internal ID20761161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77963483..78092228hg38UCSC Ensembl
chr14:78429826..78558571hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38128746
hg19128746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484819
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194121
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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