A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897590



Internal ID22672694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47936364..47944241hg38UCSC Ensembl
chr3:47977854..47985731hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg387878
hg197878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420272
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897590
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