A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846873



Internal ID22621808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44786582..44789107hg38UCSC Ensembl
chr7:44826181..44828706hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382526
hg192526
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846873
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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