A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258497



Internal ID21400413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38773265..38789228hg38UCSC Ensembl
chr19:39263905..39279868hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3815964
hg1915964
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730253
Supporting Variants
SamplesNA19239
Known GenesLGALS7, LGALS7B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258497
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