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nsv5456068

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:469

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 17 studies. See in: genome view    
Submitted genomic75,526,512-75,526,980Question Mark
Overlapping variant regions from other studies: 105 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):74,822,337-74,822,805Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5456068Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr575,526,51275,526,980
nsv5456068RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr574,822,33774,822,805

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16967121deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16967121Submitted genomicNC_000005.10:g.755
26512_75526980del
GRCh38 (hg38)NC_000005.10Chr575,526,51275,526,980
nssv16967121RemappedPerfectNC_000005.9:g.7482
2337_74822805del
GRCh37.p13First PassNC_000005.9Chr574,822,33774,822,805

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)
nssv16967121<0.00116404
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