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nsv5409405

  • 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: 76 SVs from 17 studies. See in: genome view    
Submitted genomic60,973,718-60,973,769Question Mark
Overlapping variant regions from other studies: 76 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):62,733,476-62,733,527Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5409405Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1060,973,71860,973,769
nsv5409405RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1062,733,47662,733,527

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17033894alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17033894Submitted genomicNC_000010.11:g.609
73718_60973769ins1
16
GRCh38 (hg38)NC_000010.11Chr1060,973,71860,973,769
nssv17033894RemappedPerfectNC_000010.10:g.627
33476_62733527ins1
16
GRCh37.p13First PassNC_000010.10Chr1062,733,47662,733,527

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)
nssv17033894<0.00156404
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