A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733161



Internal ID20509088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88616025..88616122hg38UCSC Ensembl
chr5:87911843..87911940hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295416
Samples
Known GenesLINC00461
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733161
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