A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848084



Internal ID22623019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:78839642..78842306hg38UCSC Ensembl
chr12:79233422..79236086hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg382665
hg192665
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848084
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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