A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847245



Internal ID22622180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:60971716..60980936hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg389221
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508318, nssv17500562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847245
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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