A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846923



Internal ID22621858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3139833..3147380hg38UCSC Ensembl
chr7:3179467..3187014hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg387548
hg197548
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505476, nssv17505475
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846923
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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