A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219329



Internal ID20786369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:14766768..14809646hg38UCSC Ensembl
chr8:14624277..14667155hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3842879
hg1942879
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416666
Supporting Variants
Samples
Known GenesSGCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219329
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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