A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183401



Internal ID20750441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76514840..76544733hg38UCSC Ensembl
chr12:76908620..76938513hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg3829894
hg1929894
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460173
Supporting Variants
Samples
Known GenesOSBPL8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183401
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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