A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230784



Internal ID20797824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21421134..21435213hg38UCSC Ensembl
chr7:21460752..21474831hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3814080
hg1914080
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618887
Supporting Variants
Samples
Known GenesSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230784
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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