A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860712



Internal ID22635647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106320425..106323424hg38UCSC Ensembl
chr12:106714203..106717202hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469447
Samples
Known GenesTCP11L2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860712
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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