A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090405



Internal ID21506297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:13796578..13796578hg38UCSC Ensembl
chr17:13699895..13699895hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658889
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090405
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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