A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867204



Internal ID22642139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46374569..46375867hg38UCSC Ensembl
chr12:46768352..46769650hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg381299
hg191299
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv407n209
Supporting Variantsnssv17465807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867204
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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