A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469825



Internal ID21127378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8786601..8795200hg38UCSC Ensembl
chr12:8939197..8947796hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg388600
hg198600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1391n223
Supporting Variantsnssv18194704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469825
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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