A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256424



Internal ID21399885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195733327..195932478hg38UCSC Ensembl
chr3:195460198..195659349hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38199152
hg19199152
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730152
Supporting Variants
SamplesNA19238
Known GenesMIR6829, MUC20, MUC4, TNK2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256424
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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