A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407289



Internal ID21064842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43721933..43727424hg38UCSC Ensembl
chr6:43689670..43695161hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385492
hg195492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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