A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218592



Internal ID20785632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1066062..1083382hg38UCSC Ensembl
chr7:1105698..1123018hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3817321
hg1917321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613939
Supporting Variants
Samples
Known GenesC7orf50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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