A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644210



Internal ID21592515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168793123..168793123hg38UCSC Ensembl
chr4:169714274..169714274hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126992
SamplesHG02818
Known GenesPALLD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644210
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