A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18001786



Internal ID20568826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55462470..55474738hg38UCSC Ensembl
chr12:55856254..55868522hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg3812269
hg1912269
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459593
Supporting Variants
Samples
Known GenesOR6C70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18001786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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