A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757545



Internal ID20533405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43322311..43388275hg38UCSC Ensembl
chr17:41399674..41465643hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3865965
hg1965970
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv45n199
Supporting Variantsnssv16270012
Samples
Known GenesLINC00910
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757545
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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