A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264620



Internal ID20831660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41335614..41336014hg38UCSC Ensembl
chr4:41337631..41338031hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264620
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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