A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094193



Internal ID21505891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20265699..20265699hg38UCSC Ensembl
chr17:20169012..20169012hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664157
Supporting Variants
SamplesNA19983
Known GenesSPECC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094193
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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