A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5604669



Internal ID21519929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100970372..100970372hg38UCSC Ensembl
chr4:101891529..101891529hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138570
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5604669
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