A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759212



Internal ID20535072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173735989..173735989hg38UCSC Ensembl
chr5:173162992..173162992hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286990
Samples
Known GenesLOC101928136
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759212
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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