A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464344



Internal ID21121897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92944385..92952927hg38UCSC Ensembl
chr12:93338161..93346703hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg388543
hg198543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464344
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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