A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936355



Internal ID22711708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101507001..101507066hg38UCSC Ensembl
chr12:101900779..101900844hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17363427
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936355
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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