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nsv5598863

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,578

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 209 SVs from 49 studies. See in: genome view    
Submitted genomic46,119,477-46,125,054Question Mark
Overlapping variant regions from other studies: 209 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):46,622,734-46,628,311Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5598863Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1946,119,47746,125,054
nsv5598863RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1946,622,73446,628,311

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17105422deletionSAMN00801888SequencingSequence alignment2,004

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17105422Submitted genomicNC_000019.10:g.461
19477_46125054delA
GRCh38 (hg38)NC_000019.10Chr1946,119,47746,125,054
nssv17105422RemappedPerfectNC_000019.9:g.4662
2734_46628311delA
GRCh37.p13First PassNC_000019.9Chr1946,622,73446,628,311

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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