A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127780



Internal ID21483789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85013916..85013977hg38UCSC Ensembl
chr3:85063067..85063128hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579329
Supporting Variants
SamplesNA12329
Known GenesCADM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127780
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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