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nsv5509459

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:159

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 81 SVs from 25 studies. See in: genome view    
Submitted genomic49,095,437-49,095,595Question Mark
Overlapping variant regions from other studies: 81 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):49,489,220-49,489,378Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5509459Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1249,095,43749,095,595
nsv5509459RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1249,489,22049,489,378

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058230deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058230Submitted genomicNC_000012.12:g.490
95437_49095595del
GRCh38 (hg38)NC_000012.12Chr1249,095,43749,095,595
nssv17058230RemappedPerfectNC_000012.11:g.494
89220_49489378del
GRCh37.p13First PassNC_000012.11Chr1249,489,22049,489,378

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)
nssv170582300.005356404
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