A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189277



Internal ID20756317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64333782..64374306hg38UCSC Ensembl
chr14:64800500..64841024hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3840525
hg1940525
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486820
Supporting Variants
Samples
Known GenesESR2, MIR548AZ, TEX21P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189277
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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