A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477929



Internal ID21135482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132564882..132596943hg38UCSC Ensembl
chr12:133141468..133173529hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3832062
hg1932062
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186191
Samples
Known GenesFBRSL1, MIR6763
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477929
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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