A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397117



Internal ID21054670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89906168..89919926hg38UCSC Ensembl
chr6:90615887..90629645hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3813759
hg1913759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397117
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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