nsv819715

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:22

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 74 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):48,588,792-48,588,813Question Mark
Overlapping variant regions from other studies: 74 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):47,205,330-47,205,351Question Mark
Overlapping variant regions from other studies: 18 SVs from 7 studies. See in: genome view    
Submitted genomic46,638,737-46,638,758Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv819715RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000020.11Chr2048,588,79248,588,813
nsv819715RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000020.10Chr2047,205,33047,205,351
nsv819715Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000020.9Chr2046,638,73746,638,758

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1418905insertionSAMN00002681SequencingPaired-end mapping1,318

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1418905RemappedPerfectNC_000020.11:g.(48
588792_?)_(?_48588
813)ins1824
GRCh38 (hg38)First PassNC_000020.11Chr2048,588,79248,588,813
nssv1418905RemappedPerfectNC_000020.10:g.(47
205330_?)_(?_47205
351)ins1824
GRCh37 (hg19)First PassNC_000020.10Chr2047,205,33047,205,351
nssv1418905Submitted genomicNC_000020.9:g.(466
38737_?)_(?_466387
58)ins1824
NCBI36 (hg18)NC_000020.9Chr2046,638,73746,638,758

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

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