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nsv5399692

  • 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: 72 SVs from 21 studies. See in: genome view    
Submitted genomic54,535,198-54,535,249Question Mark
Overlapping variant regions from other studies: 72 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):53,831,028-53,831,079Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5399692Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr554,535,19854,535,249
nsv5399692RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr553,831,02853,831,079

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16965603alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16965603Submitted genomicNC_000005.10:g.545
35198_54535249ins2
81
GRCh38 (hg38)NC_000005.10Chr554,535,19854,535,249
nssv16965603RemappedPerfectNC_000005.9:g.5383
1028_53831079ins28
1
GRCh37.p13First PassNC_000005.9Chr553,831,02853,831,079

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)
nssv16965603<0.00116404
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