nsv3967798

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:21,910

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 30 studies. See in: genome view    
Submitted genomic59,505,129-59,527,038Question Mark
Overlapping variant regions from other studies: 114 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):59,272,602-59,294,511Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv3967798Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1159,505,12959,527,038
nsv3967798RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1159,272,60259,294,511

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15211261deletionOptical mappingOptical mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv15211261Submitted genomicNC_000011.10:g.(59
505129_?)_(?_59527
038)del
GRCh38 (hg38)NC_000011.10Chr1159,505,12959,527,038
nssv15211261RemappedPerfectNC_000011.9:g.(592
72602_?)_(?_592945
11)del
GRCh37.p13First PassNC_000011.9Chr1159,272,60259,294,511

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

Support Center