A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407296



Internal ID21064849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35703292..35748350hg38UCSC Ensembl
chr6:35671069..35716127hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3845059
hg1945059
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220764
Samples
Known GenesARMC12, FKBP5, LOC285847
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407296
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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