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nsv4578204

  • 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: 59 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):45,148,898-45,148,898Question Mark
Overlapping variant regions from other studies: 59 SVs from 5 studies. See in: genome view    
Submitted genomic45,723,033-45,723,033Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578204RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1345,148,89845,148,898
nsv4578204Submitted genomicGRCh37.p13Primary AssemblyNC_000013.10Chr1345,723,03345,723,033

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16003250sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16003250RemappedPerfectNC_000013.11:g.451
48898_45148899ins5
92
GRCh38.p12First PassNC_000013.11Chr1345,148,89845,148,898
nssv16003250Submitted genomicNC_000013.10:g.457
23033_45723034ins5
92
GRCh37.p13NC_000013.10Chr1345,723,03345,723,033

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)
nssv160032504.6e-005121694
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