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nsv5449502

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:326

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 92 SVs from 17 studies. See in: genome view    
Submitted genomic170,534,326-170,534,651Question Mark
Overlapping variant regions from other studies: 92 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):170,252,115-170,252,440Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449502Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3170,534,326170,534,651
nsv5449502RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3170,252,115170,252,440

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16941835deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16941835Submitted genomicNC_000003.12:g.170
534326_170534651de
l
GRCh38 (hg38)NC_000003.12Chr3170,534,326170,534,651
nssv16941835RemappedPerfectNC_000003.11:g.170
252115_170252440de
l
GRCh37.p13First PassNC_000003.11Chr3170,252,115170,252,440

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)
nssv16941835<0.00116404
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