A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666068



Internal ID21614373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181305636..181528258hg38UCSC Ensembl
chr5:180732637..180905260hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38222623
hg19172624
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128688
SamplesHG00513
Known GenesLOC100132062, LOC100132287, LOC100133331, OR4F16, OR4F29, OR4F3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666068
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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