A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461755



Internal ID21119308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6540101..6542000hg38UCSC Ensembl
chr12:6649267..6651166hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187468
Samples
Known GenesIFFO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461755
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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