A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477966



Internal ID21135519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110388929..110389808hg38UCSC Ensembl
chr12:110826734..110827613hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38880
hg19880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193268
Samples
Known GenesANAPC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477966
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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