A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856375



Internal ID22631310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:82760754..82773987hg38UCSC Ensembl
chr12:83154533..83167766hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3813234
hg1913234
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461977
Samples
Known GenesTMTC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856375
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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