A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608884



Internal ID20981955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107433546..107434780hg38UCSC Ensembl
chr7:107073991..107075225hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146964
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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