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nsv5501992

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:424,670

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1215 SVs from 79 studies. See in: genome view    
Submitted genomic83,636,250-84,060,919Question Mark
Overlapping variant regions from other studies: 1215 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):84,030,029-84,454,698Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5501992Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1283,636,25084,060,919
nsv5501992RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1284,030,02984,454,698

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17689648duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17689648Submitted genomicNC_000012.12:g.836
36250_84060919dup
GRCh38 (hg38)NC_000012.12Chr1283,636,25084,060,919
nssv17689648RemappedPerfectNC_000012.11:g.840
30029_84454698dup
GRCh37.p13First PassNC_000012.11Chr1284,030,02984,454,698

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)
nssv17689648<0.00116404
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