A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606025



Internal ID20979096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:145117071..145117458hg38UCSC Ensembl
chr6:145438207..145438594hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38388
hg19388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140919
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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