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nsv5556566

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view    
Submitted genomic90,161,136-90,161,186Question Mark
Overlapping variant regions from other studies: 122 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):89,456,953-89,457,003Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5556566Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr590,161,13690,161,186
nsv5556566RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr589,456,95389,457,003

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16971318line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16971318Submitted genomicNC_000005.10:g.901
61136_90161186ins8
93
GRCh38 (hg38)NC_000005.10Chr590,161,13690,161,186
nssv16971318RemappedPerfectNC_000005.9:g.8945
6953_89457003ins89
3
GRCh37.p13First PassNC_000005.9Chr589,456,95389,457,003

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)
nssv16971318<0.00116404
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