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nsv5407699

  • 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: 120 SVs from 18 studies. See in: genome view    
Submitted genomic190,297,858-190,297,909Question Mark
Overlapping variant regions from other studies: 120 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):191,162,584-191,162,635Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5407699Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2190,297,858190,297,909
nsv5407699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2191,162,584191,162,635

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16923486alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16923486Submitted genomicNC_000002.12:g.190
297858_190297909in
s281
GRCh38 (hg38)NC_000002.12Chr2190,297,858190,297,909
nssv16923486RemappedPerfectNC_000002.11:g.191
162584_191162635in
s281
GRCh37.p13First PassNC_000002.11Chr2191,162,584191,162,635

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)
nssv16923486<0.00126404
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