A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229807



Internal ID20796848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148870822..148878998hg38UCSC Ensembl
chr7:148567914..148576090hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg388177
hg198177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429751
Supporting Variants
Samples
Known GenesEZH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229807
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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