A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256833



Internal ID21400220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187416752..187424678hg38UCSC Ensembl
chr3:187134540..187142466hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg387927
hg197927
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730103
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256833
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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