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nsv5420484

  • 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: 82 SVs from 20 studies. See in: genome view    
Submitted genomic24,951,696-24,951,747Question Mark
Overlapping variant regions from other studies: 82 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):24,963,017-24,963,068Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5420484Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1624,951,69624,951,747
nsv5420484RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1624,963,01724,963,068

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17706594alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17706594Submitted genomicNC_000016.10:g.249
51696_24951747ins2
66
GRCh38 (hg38)NC_000016.10Chr1624,951,69624,951,747
nssv17706594RemappedPerfectNC_000016.9:g.2496
3017_24963068ins26
6
GRCh37.p13First PassNC_000016.9Chr1624,963,01724,963,068

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)
nssv17706594<0.00116404
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