A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218980



Internal ID20786020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148795962..148804659hg38UCSC Ensembl
chr7:148493054..148501751hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg388698
hg198698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416135
Supporting Variants
Samples
Known GenesCUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218980
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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