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nsv5561064

  • 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: 78 SVs from 17 studies. See in: genome view    
Submitted genomic47,823,279-47,823,330Question Mark
Overlapping variant regions from other studies: 78 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):47,791,015-47,791,066Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5561064Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr647,823,27947,823,330
nsv5561064RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr647,791,01547,791,066

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16981518line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16981518Submitted genomicNC_000006.12:g.478
23279_47823330ins1
198
GRCh38 (hg38)NC_000006.12Chr647,823,27947,823,330
nssv16981518RemappedPerfectNC_000006.11:g.477
91015_47791066ins1
198
GRCh37.p13First PassNC_000006.11Chr647,791,01547,791,066

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)
nssv16981518<0.00166402
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