A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620755



Internal ID21569060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3043470..3043470hg38UCSC Ensembl
chr2:3047242..3047242hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17114107
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620755
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