A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531220



Internal ID21855576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:54720947..54721170hg38UCSC Ensembl
chr2:54948084..54948307hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531220
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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