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nsv5087945

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 95 SVs from 21 studies. See in: genome view    
Submitted genomic152,397,012-152,397,031Question Mark
Overlapping variant regions from other studies: 95 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):151,776,573-151,776,592Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5087945Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5152,397,012152,397,031
nsv5087945RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5151,776,573151,776,592

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16643825alu insertionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16643825Submitted genomicNC_000005.10:g.152
397012_152397031in
s68
GRCh38 (hg38)NC_000005.10Chr5152,397,012152,397,031
nssv16643825RemappedPerfectNC_000005.9:g.1517
76573_151776592ins
68
GRCh37.p13First PassNC_000005.9Chr5151,776,573151,776,592

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)
nssv166438250.4
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