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nsv5407766

  • 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: 132 SVs from 25 studies. See in: genome view    
Submitted genomic58,184,620-58,184,671Question Mark
Overlapping variant regions from other studies: 132 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):58,411,755-58,411,806Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5407766Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr258,184,62058,184,671
nsv5407766RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr258,411,75558,411,806

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16913547alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16913547Submitted genomicNC_000002.12:g.581
84620_58184671ins2
81
GRCh38 (hg38)NC_000002.12Chr258,184,62058,184,671
nssv16913547RemappedPerfectNC_000002.11:g.584
11755_58411806ins2
81
GRCh37.p13First PassNC_000002.11Chr258,411,75558,411,806

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)
nssv16913547<0.00116404
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