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nsv5448313

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,321

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 221 SVs from 32 studies. See in: genome view    
Submitted genomic237,401,367-237,406,687Question Mark
Overlapping variant regions from other studies: 221 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):238,310,010-238,315,330Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5448313Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2237,401,367237,406,687
nsv5448313RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2238,310,010238,315,330

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16926419deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16926419Submitted genomicNC_000002.12:g.237
401367_237406687de
l
GRCh38 (hg38)NC_000002.12Chr2237,401,367237,406,687
nssv16926419RemappedPerfectNC_000002.11:g.238
310010_238315330de
l
GRCh37.p13First PassNC_000002.11Chr2238,310,010238,315,330

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)
nssv16926419<0.00146404
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