A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220227



Internal ID20787267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6815601..6821800hg38UCSC Ensembl
chr7:6855232..6861431hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615365
Supporting Variants
Samples
Known GenesCCZ1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220227
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.05219


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