A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464423



Internal ID21121976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:60683556..60722099hg38UCSC Ensembl
chr12:61077337..61115880hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3838544
hg1938544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464423
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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