A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846886



Internal ID22621821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:48067740..48075899hg38UCSC Ensembl
chr7:48107337..48115496hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg388160
hg198160
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17507105, nssv17507106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846886
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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