A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463355



Internal ID21120908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:64401501..64407000hg38UCSC Ensembl
chr12:64795281..64800780hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193714
Samples
Known GenesXPOT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463355
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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