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nsv5515054

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:364

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 101 SVs from 17 studies. See in: genome view    
Submitted genomic42,013,875-42,014,238Question Mark
Overlapping variant regions from other studies: 101 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):42,518,027-42,518,390Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5515054Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1942,013,87542,014,238
nsv5515054RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1942,518,02742,518,390

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17725097deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17725097Submitted genomicNC_000019.10:g.420
13875_42014238del
GRCh38 (hg38)NC_000019.10Chr1942,013,87542,014,238
nssv17725097RemappedPerfectNC_000019.9:g.4251
8027_42518390del
GRCh37.p13First PassNC_000019.9Chr1942,518,02742,518,390

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)
nssv17725097<0.00126404
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