A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851611



Internal ID22626546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32677069..32678691hg38UCSC Ensembl
chr12:32830003..32831625hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg381623
hg191623
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851611
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer