A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17111402



Internal ID21402286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202103857..202103857hg38UCSC Ensembl
chr2:202968580..202968580hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38846
hg19846
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608749
Supporting Variants
SamplesHG00096
Known GenesLOC100652824
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17111402
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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