A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638990



Internal ID21587295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:34969324..34969324hg38UCSC Ensembl
chr7:35008936..35008936hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147389
SamplesNA18939
Known GenesDPY19L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638990
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