A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914206



Internal ID22689423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32420529..32453820hg38UCSC Ensembl
chr12:32573463..32606754hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3833292
hg1933292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361685
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914206
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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