A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226085



Internal ID20793125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80675206..80793905hg38UCSC Ensembl
chr7:80304522..80423221hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38118700
hg19118700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610551
Supporting Variants
Samples
Known GenesCD36, SEMA3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226085
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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