A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189361



Internal ID20756401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22771990..22772381hg38UCSC Ensembl
chr14:23241199..23241590hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477151
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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