A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109903



Internal ID21442457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17753324..17753324hg38UCSC Ensembl
chr2:17934591..17934591hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617920
Supporting Variants
SamplesHG00732
Known GenesSMC6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109903
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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