A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087981



Internal ID21458077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27351845..27351845hg38UCSC Ensembl
chr17:25678871..25678871hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648054
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087981
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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