A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184781



Internal ID20751821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64589247..64589800hg38UCSC Ensembl
chr12:64983027..64983580hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184781
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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