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nsv5489209

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:93

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 108 SVs from 26 studies. See in: genome view    
Submitted genomic107,796,700-107,796,792Question Mark
Overlapping variant regions from other studies: 108 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):107,437,145-107,437,237Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489209Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7107,796,700107,796,792
nsv5489209RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7107,437,145107,437,237

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17004053deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17004053Submitted genomicNC_000007.14:g.107
796700_107796792de
l
GRCh38 (hg38)NC_000007.14Chr7107,796,700107,796,792
nssv17004053RemappedPerfectNC_000007.13:g.107
437145_107437237de
l
GRCh37.p13First PassNC_000007.13Chr7107,437,145107,437,237

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)
nssv170040530.014896402
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