A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088027



Internal ID21459622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60397960..60397960hg38UCSC Ensembl
chr17:58475321..58475321hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381244
hg191244
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5661377
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088027
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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