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nsv5446254

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:250

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 195 SVs from 38 studies. See in: genome view    
Submitted genomic131,604,686-131,604,935Question Mark
Overlapping variant regions from other studies: 195 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):132,362,259-132,362,508Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5446254Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2131,604,686131,604,935
nsv5446254RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2132,362,259132,362,508

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16917844deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16917844Submitted genomicNC_000002.12:g.131
604686_131604935de
l
GRCh38 (hg38)NC_000002.12Chr2131,604,686131,604,935
nssv16917844RemappedPerfectNC_000002.11:g.132
362259_132362508de
l
GRCh37.p13First PassNC_000002.11Chr2132,362,259132,362,508

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)
nssv169178440.003206404
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