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nsv5440341

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:134

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 21 studies. See in: genome view    
Submitted genomic170,532,169-170,532,302Question Mark
Overlapping variant regions from other studies: 99 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):170,249,958-170,250,091Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5440341Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3170,532,169170,532,302
nsv5440341RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3170,249,958170,250,091

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16941834deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16941834Submitted genomicNC_000003.12:g.170
532169_170532302de
l
GRCh38 (hg38)NC_000003.12Chr3170,532,169170,532,302
nssv16941834RemappedPerfectNC_000003.11:g.170
249958_170250091de
l
GRCh37.p13First PassNC_000003.11Chr3170,249,958170,250,091

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)
nssv169418340.002156404
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