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nsv5424970

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 22 studies. See in: genome view    
Submitted genomic19,672,502-19,672,586Question Mark
Overlapping variant regions from other studies: 94 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):19,998,995-19,999,079Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424970Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr119,672,50219,672,586
nsv5424970RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr119,998,99519,999,079

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16902244deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16902244Submitted genomicNC_000001.11:g.196
72502_19672586del
GRCh38 (hg38)NC_000001.11Chr119,672,50219,672,586
nssv16902244RemappedPerfectNC_000001.10:g.199
98995_19999079del
GRCh37.p13First PassNC_000001.10Chr119,998,99519,999,079

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)
nssv16902244<0.00116404
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