A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405093



Internal ID21062646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63493606..63499952hg38UCSC Ensembl
chr6:64203511..64209857hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg386347
hg196347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142976
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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