A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414458



Internal ID21072011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33252361..33301396hg38UCSC Ensembl
chr6:33220138..33269173hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3849036
hg1949036
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231823
Samples
Known GenesB3GALT4, HCG25, MIR6834, MIR6873, PFDN6, RGL2, RPS18, TAPBP, VPS52, WDR46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414458
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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