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nsv5412847

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 25 studies. See in: genome view    
Submitted genomic161,019,993-161,020,003Question Mark
Overlapping variant regions from other studies: 129 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):160,989,783-160,989,793Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5412847Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1161,019,993161,020,003
nsv5412847RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,989,783160,989,793

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892354alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892354Submitted genomicNC_000001.11:g.161
019993_161020003in
s259
GRCh38 (hg38)NC_000001.11Chr1161,019,993161,020,003
nssv16892354RemappedPerfectNC_000001.10:g.160
989783_160989793in
s259
GRCh37.p13First PassNC_000001.10Chr1160,989,783160,989,793

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)
nssv16892354<0.00116404
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