A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257433



Internal ID21398999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187414749..187426653hg38UCSC Ensembl
chr3:187132537..187144441hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3811905
hg1911905
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730103
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257433
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer