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nsv5552584

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 20 studies. See in: genome view    
Submitted genomic155,017,363-155,017,398Question Mark
Overlapping variant regions from other studies: 122 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):154,989,839-154,989,874Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5552584Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1155,017,363155,017,398
nsv5552584RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1154,989,839154,989,874

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890423insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890423Submitted genomicNC_000001.11:g.155
017363_155017398in
s53
GRCh38 (hg38)NC_000001.11Chr1155,017,363155,017,398
nssv16890423RemappedPerfectNC_000001.10:g.154
989839_154989874in
s53
GRCh37.p13First PassNC_000001.10Chr1154,989,839154,989,874

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)
nssv168904230.1348426294
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