A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851591



Internal ID22626526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:50378775..50381916hg38UCSC Ensembl
chr12:50772558..50775699hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg383142
hg193142
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452978
Samples
Known GenesFAM186A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851591
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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