A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293353



Internal ID20502571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43304237..43386202hg38UCSC Ensembl
chr17:41381586..41463570hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3881966
hg1981985
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759534
Supporting Variants
Samples
Known GenesLINC00910
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293353
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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