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nsv5437927

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:59

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 32 studies. See in: genome view    
Submitted genomic165,050,402-165,050,460Question Mark
Overlapping variant regions from other studies: 162 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):164,768,190-164,768,248Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5437927Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3165,050,402165,050,460
nsv5437927RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3164,768,190164,768,248

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16942115deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16942115Submitted genomicNC_000003.12:g.165
050402_165050460de
l
GRCh38 (hg38)NC_000003.12Chr3165,050,402165,050,460
nssv16942115RemappedPerfectNC_000003.11:g.164
768190_164768248de
l
GRCh37.p13First PassNC_000003.11Chr3164,768,190164,768,248

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)
nssv16942115<0.00126404
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