A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539152



Internal ID20912459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101811839..101812813hg38UCSC Ensembl
chr3:101530683..101531657hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38975
hg19975
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259491
Samples
Known GenesNXPE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539152
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