A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063284



Internal ID21512762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234204871..234222346hg38UCSC Ensembl
chr1:234340617..234358092hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3817476
hg1917476
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670737
Supporting Variants
Samples
Known GenesSLC35F3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063284
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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