A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851959



Internal ID22626894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32422047..32429680hg38UCSC Ensembl
chr12:32574981..32582614hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg387634
hg197634
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv359n209
Supporting Variantsnssv17452040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851959
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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