nsv4531589

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,087

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 48 SVs from 10 studies. See in: genome view    
Remapped(Score: Perfect):38,843,144-38,846,230Question Mark
Overlapping variant regions from other studies: 45 SVs from 10 studies. See in: genome view    
Submitted genomic36,999,397-37,002,483Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4531589RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1738,843,14438,846,230
nsv4531589Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1736,999,39737,002,483

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15836203deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15836203RemappedPerfectNC_000017.11:g.388
43144_38846230del		GRCh38.p12First PassNC_000017.11Chr1738,843,14438,846,230
nssv15836203Submitted genomicNC_000017.10:g.369
99397_37002483del		GRCh37.p13NC_000017.10Chr1736,999,39737,002,483

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)
nssv15836203<0.001521694
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