A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17122455



Internal ID21465469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196470185..196470259hg38UCSC Ensembl
chr3:196197056..196197130hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5574523
Supporting Variants
SamplesHG03065
Known GenesRNF168
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17122455
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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