A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488622



Internal ID21146175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109919283..109922833hg38UCSC Ensembl
chr12:110357088..110360638hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg383551
hg193551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488622
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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