A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644952



Internal ID21593257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70312975..70312975hg38UCSC Ensembl
chr17:68309116..68309116hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089003
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644952
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