A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431787



Internal ID21393789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5431567..5432565hg38UCSC Ensembl
chr12:5540733..5541731hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv154n172
Supporting Variantsnssv15746671
SamplesSMI034
Known GenesNTF3
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431787
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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