A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595519



Internal ID20968590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96595768..96596328hg38UCSC Ensembl
chr14:97062105..97062665hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238400
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595519
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