A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115333



Internal ID21401935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9700490..9700490hg38UCSC Ensembl
chr2:9840619..9840619hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg386147
hg196147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622245
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115333
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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