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nsv5425232

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 19 studies. See in: genome view    
Submitted genomic151,808,871-151,808,955Question Mark
Overlapping variant regions from other studies: 110 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):151,781,347-151,781,431Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5425232Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1151,808,871151,808,955
nsv5425232RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1151,781,347151,781,431

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16889222deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16889222Submitted genomicNC_000001.11:g.151
808871_151808955de
l
GRCh38 (hg38)NC_000001.11Chr1151,808,871151,808,955
nssv16889222RemappedPerfectNC_000001.10:g.151
781347_151781431de
l
GRCh37.p13First PassNC_000001.10Chr1151,781,347151,781,431

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)
nssv16889222<0.00116404
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