A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857218



Internal ID22632153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45392990..45395179hg38UCSC Ensembl
chr12:45786773..45788962hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg382190
hg192190
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456269
Samples
Known GenesANO6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857218
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