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nsv5401473

  • 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: 88 SVs from 12 studies. See in: genome view    
Submitted genomic63,720,880-63,720,931Question Mark
Overlapping variant regions from other studies: 88 SVs from 12 studies. See in: genome view    
Remapped(Score: Perfect):64,430,776-64,430,827Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5401473Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr663,720,88063,720,931
nsv5401473RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr664,430,77664,430,827

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17735535alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17735535Submitted genomicNC_000006.12:g.637
20880_63720931ins2
67
GRCh38 (hg38)NC_000006.12Chr663,720,88063,720,931
nssv17735535RemappedPerfectNC_000006.11:g.644
30776_64430827ins2
67
GRCh37.p13First PassNC_000006.11Chr664,430,77664,430,827

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)
nssv17735535<0.00126404
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