A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559818



Internal ID20932889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150151768..150152304hg38UCSC Ensembl
chr4:151072920..151073456hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5515n223
Supporting Variantsnssv18263780
Samples
Known GenesDCLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559818
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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