A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188419



Internal ID20755459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31994468..32006980hg38UCSC Ensembl
chr12:32147402..32159914hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3812513
hg1912513
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467951
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188419
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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