A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460280



Internal ID21117833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57377028..57387220hg38UCSC Ensembl
chr12:57770811..57781003hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg3810193
hg1910193
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188280
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460280
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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