A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147442



Internal ID21506399
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 StatusS
Merged Variantsnsv5665864
Supporting Variants
SamplesNA19983
Known GenesC6orf163
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147442
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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