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nsv5416754

  • 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: 178 SVs from 26 studies. See in: genome view    
Submitted genomic41,271,238-41,271,289Question Mark
Overlapping variant regions from other studies: 178 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):42,643,165-42,643,216Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5416754Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000021.9Chr2141,271,23841,271,289
nsv5416754RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000021.8Chr2142,643,16542,643,216

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17726988alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17726988Submitted genomicNC_000021.9:g.4127
1238_41271289ins28
0
GRCh38 (hg38)NC_000021.9Chr2141,271,23841,271,289
nssv17726988RemappedPerfectNC_000021.8:g.4264
3165_42643216ins28
0
GRCh37.p13First PassNC_000021.8Chr2142,643,16542,643,216

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)
nssv177269880.0231486404
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