A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459058



Internal ID21116611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21656201..21681800hg38UCSC Ensembl
chr12:21809135..21834734hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3825600
hg1925600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180289
Samples
Known GenesLDHB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459058
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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