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nsv5198694

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 130 SVs from 38 studies. See in: genome view    
Submitted genomic107,770,230-107,770,268Question Mark
Overlapping variant regions from other studies: 130 SVs from 38 studies. See in: genome view    
Remapped(Score: Perfect):107,410,675-107,410,713Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5198694Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7107,770,230107,770,268
nsv5198694RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7107,410,675107,410,713

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16659539line1 insertionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16659539Submitted genomicNC_000007.14:g.107
770230_107770268in
s379
GRCh38 (hg38)NC_000007.14Chr7107,770,230107,770,268
nssv16659539RemappedPerfectNC_000007.13:g.107
410675_107410713in
s379
GRCh37.p13First PassNC_000007.13Chr7107,410,675107,410,713

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)
nssv166595390.996
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