A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179253



Internal ID20746293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61099801..61201342hg38UCSC Ensembl
chr14:61566519..61668060hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38101542
hg19101542
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478201
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179253
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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