A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110077



Internal ID21425066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216766166..216766166hg38UCSC Ensembl
chr2:217630889..217630889hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618483
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110077
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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