A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179911



Internal ID20746951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107032615..107110756hg38UCSC Ensembl
chr12:107426393..107504534hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3878142
hg1978142
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469703
Supporting Variants
Samples
Known GenesCRY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179911
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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