A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470298



Internal ID21127851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8784901..8795600hg38UCSC Ensembl
chr12:8937497..8948196hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1391n223
Supporting Variantsnssv18183458
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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