A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409389



Internal ID21066942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6801438..6810825hg38UCSC Ensembl
chr6:6801671..6811058hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg389388
hg199388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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