A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406608



Internal ID21064161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85446101..85449400hg38UCSC Ensembl
chr6:86155819..86159118hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406608
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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