A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850633



Internal ID22625568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107532965..107535535hg38UCSC Ensembl
chr7:107173410..107175980hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg382571
hg192571
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500108
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850633
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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