A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612868



Internal ID20985939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99853674..99854074hg38UCSC Ensembl
chr7:99451297..99451697hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162450
Samples
Known GenesCYP3A43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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