A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467951



Internal ID21125504
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 StatusM
Merged Variants
Supporting Variantsnssv18188419
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467951
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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