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nsv5548463

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:471

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 201 SVs from 21 studies. See in: genome view    
Submitted genomic45,939,745-45,940,215Question Mark
Overlapping variant regions from other studies: 201 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):46,335,625-46,336,095Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5548463Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2245,939,74545,940,215
nsv5548463RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2246,335,62546,336,095

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17729519deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17729519Submitted genomicNC_000022.11:g.459
39745_45940215del
GRCh38 (hg38)NC_000022.11Chr2245,939,74545,940,215
nssv17729519RemappedPerfectNC_000022.10:g.463
35625_46336095del
GRCh37.p13First PassNC_000022.10Chr2246,335,62546,336,095

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17729519<0.00116404
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