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nsv5494028

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:603,344

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1640 SVs from 81 studies. See in: genome view    
Submitted genomic74,225,600-74,828,943Question Mark
Overlapping variant regions from other studies: 1640 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):73,936,645-74,539,988Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5494028Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1174,225,60074,828,943
nsv5494028RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1173,936,64574,539,988

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17048382duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17048382Submitted genomicNC_000011.10:g.742
25600_74828943dup
GRCh38 (hg38)NC_000011.10Chr1174,225,60074,828,943
nssv17048382RemappedPerfectNC_000011.9:g.7393
6645_74539988dup
GRCh37.p13First PassNC_000011.9Chr1173,936,64574,539,988

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)
nssv17048382<0.00126404
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