A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189672



Internal ID20756712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95242372..95253687hg38UCSC Ensembl
chr14:95708709..95720024hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3811316
hg1911316
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503286
Supporting Variants
Samples
Known GenesCLMN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189672
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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