A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465892



Internal ID21123445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:68386308..68407867hg38UCSC Ensembl
chr12:68780088..68801647hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3821560
hg1921560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465892
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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