A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262727



Internal ID20829767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96077282..96571313hg38UCSC Ensembl
chr3:95796126..96290157hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38494032
hg19494032
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546305
Supporting Variants
Samples
Known GenesMIR8060
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262727
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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