A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17112437



Internal ID21449847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239938925..239938990hg38UCSC Ensembl
chr2:240878342..240878407hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582914
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17112437
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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