A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865159



Internal ID22640094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:49290024..49296637hg38UCSC Ensembl
chr12:49683807..49690420hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg386614
hg196614
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453397
Samples
Known GenesPRPH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865159
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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