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nsv5397204

  • 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: 85 SVs from 16 studies. See in: genome view    
Submitted genomic72,135,720-72,135,771Question Mark
Overlapping variant regions from other studies: 85 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):71,431,547-71,431,598Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5397204Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr572,135,72072,135,771
nsv5397204RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr571,431,54771,431,598

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16967499alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16967499Submitted genomicNC_000005.10:g.721
35720_72135771ins2
81
GRCh38 (hg38)NC_000005.10Chr572,135,72072,135,771
nssv16967499RemappedPerfectNC_000005.9:g.7143
1547_71431598ins28
1
GRCh37.p13First PassNC_000005.9Chr571,431,54771,431,598

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)
nssv169674990.004276404
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