A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094850



Internal ID21507518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76966949..76966949hg38UCSC Ensembl
chr17:74963031..74963031hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662372
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094850
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