A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866280



Internal ID22641215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5500474..5503573hg38UCSC Ensembl
chr12:5609640..5612739hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866280
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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