A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091662



Internal ID21414159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34730224..34730224hg38UCSC Ensembl
chr17:33057243..33057243hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652553
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091662
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