A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571965



Internal ID20945036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143463455..143464378hg38UCSC Ensembl
chr4:144384608..144385531hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5481n223
Supporting Variantsnssv18264757
Samples
Known GenesGAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571965
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