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nsv4573485

  • 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: 45 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):15,430,611-15,430,611Question Mark
Overlapping variant regions from other studies: 45 SVs from 6 studies. See in: genome view    
Submitted genomic15,411,256-15,411,256Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573485RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2015,430,61115,430,611
nsv4573485Submitted genomicGRCh37.p13Primary AssemblyNC_000020.10Chr2015,411,25615,411,256

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16031143insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16031143RemappedPerfectNC_000020.11:g.154
30611_15430612ins8
1
GRCh38.p12First PassNC_000020.11Chr2015,430,61115,430,611
nssv16031143Submitted genomicNC_000020.10:g.154
11256_15411257ins8
1
GRCh37.p13NC_000020.10Chr2015,411,25615,411,256

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)
nssv16031143<0.001321694
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