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nsv5396729

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 164 SVs from 33 studies. See in: genome view    
Submitted genomic165,031,240-165,031,291Question Mark
Overlapping variant regions from other studies: 164 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):164,749,028-164,749,079Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5396729Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3165,031,240165,031,291
nsv5396729RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3164,749,028164,749,079

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16942113alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16942113Submitted genomicNC_000003.12:g.165
031240_165031291in
s281
GRCh38 (hg38)NC_000003.12Chr3165,031,240165,031,291
nssv16942113RemappedPerfectNC_000003.11:g.164
749028_164749079in
s281
GRCh37.p13First PassNC_000003.11Chr3164,749,028164,749,079

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)
nssv16942113<0.00136404
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