A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17110443



Internal ID21459762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174210598..174210598hg38UCSC Ensembl
chr2:175075326..175075326hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624366
Supporting Variants
SamplesHG02818
Known GenesOLA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17110443
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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