A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17134364



Internal ID21497839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87022550..87022603hg38UCSC Ensembl
chr4:87943702..87943755hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568905
Supporting Variants
SamplesNA19238
Known GenesAFF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17134364
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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