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nsv4510489

  • 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: 35 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):64,968,663-64,968,663Question Mark
Overlapping variant regions from other studies: 35 SVs from 4 studies. See in: genome view    
Submitted genomic65,261,000-65,261,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4510489RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1564,968,66364,968,663
nsv4510489Submitted genomicGRCh37.p13Primary AssemblyNC_000015.9Chr1565,261,00065,261,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16013184alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16013184RemappedPerfectNC_000015.10:g.649
68663_64968664ins1
34
GRCh38.p12First PassNC_000015.10Chr1564,968,66364,968,663
nssv16013184Submitted genomicNC_000015.9:g.6526
1000_65261001ins13
4
GRCh37.p13NC_000015.9Chr1565,261,00065,261,000

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)
nssv160131844.6e-005121694
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