A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586759



Internal ID20959830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3880375..3880813hg38UCSC Ensembl
chr18:3880375..3880813hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244257
Samples
Known GenesDLGAP1, DLGAP1-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586759
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