A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17131402



Internal ID21480940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33844986..33847225hg38UCSC Ensembl
chr4:33846608..33848847hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg382240
hg192240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569177
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17131402
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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