A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471843



Internal ID21129396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:53525223..53526080hg38UCSC Ensembl
chr12:53919007..53919864hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38858
hg19858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182650
Samples
Known GenesATF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471843
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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