A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625031



Internal ID21573336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:107318807..107318807hg38UCSC Ensembl
chr5:106654508..106654508hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127119
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625031
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