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nsv5411445

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 17 studies. See in: genome view    
Submitted genomic190,252,877-190,252,928Question Mark
Overlapping variant regions from other studies: 119 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):191,117,603-191,117,654Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5411445Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2190,252,877190,252,928
nsv5411445RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2191,117,603191,117,654

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16923480alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16923480Submitted genomicNC_000002.12:g.190
252877_190252928in
s268
GRCh38 (hg38)NC_000002.12Chr2190,252,877190,252,928
nssv16923480RemappedPerfectNC_000002.11:g.191
117603_191117654in
s268
GRCh37.p13First PassNC_000002.11Chr2191,117,603191,117,654

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)
nssv16923480<0.00116404
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