A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409234



Internal ID21066787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92476722..92698898hg38UCSC Ensembl
chr6:93186440..93408616hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38222177
hg19222177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148736
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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