A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638060



Internal ID21586365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181326532..181326532hg38UCSC Ensembl
chr5:180753533..180753533hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131307
SamplesHG03125
Known GenesLOC100132062, LOC100132287, LOC100133331
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638060
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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