A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277138



Internal ID20486356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47303501..47317337hg38UCSC Ensembl
chr8:48214905..48230824hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3813837
hg1915920
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761239
Supporting Variants
Samples
Known GenesSPIDR
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277138
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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