A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256100



Internal ID21400585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87926218..87937505hg38UCSC Ensembl
chr4:88847370..88858657hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3811288
hg1911288
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730077
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256100
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