A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256826



Internal ID21400672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233986..40234902hg38UCSC Ensembl
chr4:40235606..40236522hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730160
Supporting Variants
SamplesNA19240
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256826
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