A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464884



Internal ID21122437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51044276..51044787hg38UCSC Ensembl
chr12:51438059..51438570hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464884
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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