A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859595



Internal ID22634530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50116292..50124826hg38UCSC Ensembl
chr12:50510075..50518609hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg388535
hg198535
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462276
Samples
Known GenesCOX14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859595
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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