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nsv5424209

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:76

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 95 SVs from 17 studies. See in: genome view    
Submitted genomic157,030,184-157,030,259Question Mark
Overlapping variant regions from other studies: 101 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):156,999,976-157,000,051Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424209Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1157,030,184157,030,259
nsv5424209RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1156,999,976157,000,051

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890945deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890945Submitted genomicNC_000001.11:g.157
030184_157030259de
l
GRCh38 (hg38)NC_000001.11Chr1157,030,184157,030,259
nssv16890945RemappedPerfectNC_000001.10:g.156
999976_157000051de
l
GRCh37.p13First PassNC_000001.10Chr1156,999,976157,000,051

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)
nssv16890945<0.00116404
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