A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397300



Internal ID21054853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33363807..33364221hg38UCSC Ensembl
chr6:33331584..33331998hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234461
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397300
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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