A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665864



Internal ID21614170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87342793..87349945hg38UCSC Ensembl
chr6:88052511..88059663hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg387153
hg197153
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147442
SamplesNA19983
Known GenesC6orf163
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665864
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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