A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864375



Internal ID22639310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41100794..41110511hg38UCSC Ensembl
chr12:41494596..41504313hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg389718
hg199718
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864375
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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