A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17109892



Internal ID21494652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:177178710..177178762hg38UCSC Ensembl
chr2:178043438..178043490hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5582850
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17109892
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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