A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191721



Internal ID20758761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5812589..5812696hg38UCSC Ensembl
chr12:5921755..5921862hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463322
Supporting Variants
Samples
Known GenesANO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191721
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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