A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107425



Internal ID21482866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10030634..10030634hg38UCSC Ensembl
chr2:10170761..10170761hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38997
hg19997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604605
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107425
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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