A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566862



Internal ID21515193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88616032..88616130hg38UCSC Ensembl
chr5:87911850..87911948hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139642
SamplesHG00731
Known GenesLINC00461
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566862
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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