A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107290



Internal ID21494261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105209434..105211968hg38UCSC Ensembl
chr2:105825891..105828425hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg382535
hg192535
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5564627
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107290
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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