A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541669



Internal ID21866024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:188362708..189560579hg38UCSC Ensembl
chr4:189283862..190481733hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381197872
hg191197872
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100711
Supporting Variants
Samples
Known GenesLINC01060
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541669
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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