A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737649



Internal ID20513611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98504898..98511327hg38UCSC Ensembl
chr2:99121361..99127790hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg386430
hg196430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270805
Samples
Known GenesINPP4A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737649
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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