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nsv5440161

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:237

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 251 SVs from 23 studies. See in: genome view    
Submitted genomic241,148,961-241,149,197Question Mark
Overlapping variant regions from other studies: 251 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):242,088,376-242,088,612Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5440161Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2241,148,961241,149,197
nsv5440161RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2242,088,376242,088,612

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16927163deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16927163Submitted genomicNC_000002.12:g.241
148961_241149197de
l
GRCh38 (hg38)NC_000002.12Chr2241,148,961241,149,197
nssv16927163RemappedPerfectNC_000002.11:g.242
088376_242088612de
l
GRCh37.p13First PassNC_000002.11Chr2242,088,376242,088,612

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)
nssv16927163<0.00116404
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