A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852107



Internal ID22627042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142773050..142774565hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381516
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1929n209
Supporting Variantsnssv17502150, nssv17502149
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852107
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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