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nsv5556968

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 22 studies. See in: genome view    
Submitted genomic45,112,959-45,112,985Question Mark
Overlapping variant regions from other studies: 91 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):45,154,451-45,154,477Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5556968Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr345,112,95945,112,985
nsv5556968RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr345,154,45145,154,477

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933690sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933690Submitted genomicNC_000003.12:g.451
12959_45112985ins1
226
GRCh38 (hg38)NC_000003.12Chr345,112,95945,112,985
nssv16933690RemappedPerfectNC_000003.11:g.451
54451_45154477ins1
226
GRCh37.p13First PassNC_000003.11Chr345,154,45145,154,477

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)
nssv16933690<0.00136404
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