A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846568



Internal ID22621503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2349039..2351624hg38UCSC Ensembl
chr7:2388674..2391259hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg382586
hg192586
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504774
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846568
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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