A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846409



Internal ID22621344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135176..144774hg38UCSC Ensembl
chr7:135176..144774hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg389599
hg199599
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503953, nssv17501319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846409
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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