A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148584



Internal ID21512641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32645667..32647977hg38UCSC Ensembl
chr6:32613444..32615754hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg382311
hg192311
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667663
Supporting Variants
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148584
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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