A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411217



Internal ID21068770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68690190..68690837hg38UCSC Ensembl
chr6:69400082..69400729hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143832
Samples
Known GenesBAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411217
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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