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nsv4578028

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 24 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):64,912,509-64,912,509Question Mark
Overlapping variant regions from other studies: 24 SVs from 5 studies. See in: genome view    
Submitted genomic65,379,227-65,379,227Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578028RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1464,912,50964,912,509
nsv4578028Submitted genomicGRCh37.p13Primary AssemblyNC_000014.8Chr1465,379,22765,379,227

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16010333sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16010333RemappedPerfectNC_000014.9:g.6491
2509_64912510ins41
9
GRCh38.p12First PassNC_000014.9Chr1464,912,50964,912,509
nssv16010333Submitted genomicNC_000014.8:g.6537
9227_65379228ins41
9
GRCh37.p13NC_000014.8Chr1465,379,22765,379,227

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)
nssv160103334.6e-005121694
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