A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223593



Internal ID20790634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138676899..138687231hg38UCSC Ensembl
chr7:138361644..138371976hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3810333
hg1910333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430005
Supporting Variants
Samples
Known GenesSVOPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223593
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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