A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413296



Internal ID21070849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:90372872..90373218hg38UCSC Ensembl
chr6:91082591..91082937hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145386
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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