A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846701



Internal ID22621636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4624488..4633292hg38UCSC Ensembl
chr7:4664119..4672923hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg388805
hg198805
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846701
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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