A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16255940



Internal ID21398251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187418572..187424670hg38UCSC Ensembl
chr3:187136360..187142458hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg386099
hg196099
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730103
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16255940
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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