A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134006



Internal ID21475009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106073578..106074578hg38UCSC Ensembl
chr3:105792425..105793425hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569003
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134006
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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