A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17108436



Internal ID21504328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12706252..12706252hg38UCSC Ensembl
chr2:12846378..12846378hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5612771
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17108436
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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