A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616292



Internal ID20989363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107756263..107756948hg38UCSC Ensembl
chr7:107396708..107397393hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146990
Samples
Known GenesCBLL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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