A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481658



Internal ID21139211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122658993..122664145hg38UCSC Ensembl
chr12:123143540..123148692hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg385153
hg195153
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481658
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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