A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635749



Internal ID21584054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38074136..38074136hg38UCSC Ensembl
chr8:37931654..37931654hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147994, nssv17158257
SamplesHG00512, HG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635749
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer