A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852693



Internal ID22627628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31793961..31796287hg38UCSC Ensembl
chr12:31946895..31949221hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg382327
hg192327
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852693
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