A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16255965



Internal ID21399117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13104251..13158142hg38UCSC Ensembl
chr1:13171719..13219912hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3853892
hg1948194
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730073
Supporting Variants
SamplesHG00732
Known GenesHNRNPCP5
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16255965
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