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nsv4545757

  • 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: 22 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):52,810,148-52,810,148Question Mark
Overlapping variant regions from other studies: 22 SVs from 7 studies. See in: genome view    
Submitted genomic53,203,932-53,203,932Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4545757RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1252,810,14852,810,148
nsv4545757Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr1253,203,93253,203,932

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16002371insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16002371RemappedPerfectNC_000012.12:g.528
10148_52810149ins1
16
GRCh38.p12First PassNC_000012.12Chr1252,810,14852,810,148
nssv16002371Submitted genomicNC_000012.11:g.532
03932_53203933ins1
16
GRCh37.p13NC_000012.11Chr1253,203,93253,203,932

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)
nssv160023714.6e-005121694
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