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nsv5409192

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 24 studies. See in: genome view    
Submitted genomic87,914,770-87,914,770Question Mark
Overlapping variant regions from other studies: 136 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):89,674,527-89,674,527Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5409192Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1087,914,77087,914,770
nsv5409192RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1089,674,52789,674,527

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17038399alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17038399Submitted genomicNC_000010.11:g.879
14770_87914771ins3
24
GRCh38 (hg38)NC_000010.11Chr1087,914,77087,914,770
nssv17038399RemappedPerfectNC_000010.10:g.896
74527_89674528ins3
24
GRCh37.p13First PassNC_000010.10Chr1089,674,52789,674,527

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)
nssv170383990.004286402
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