A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110391



Internal ID21424917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161095805..161095805hg38UCSC Ensembl
chr2:161952316..161952316hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611938
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110391
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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