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nsv5551768

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
Submitted genomic64,588,806-64,588,850Question Mark
Overlapping variant regions from other studies: 123 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):65,054,489-65,054,533Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5551768Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr164,588,80664,588,850
nsv5551768RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr165,054,48965,054,533

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16904515insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16904515Submitted genomicNC_000001.11:g.645
88806_64588850ins8
0
GRCh38 (hg38)NC_000001.11Chr164,588,80664,588,850
nssv16904515RemappedPerfectNC_000001.10:g.650
54489_65054533ins8
0
GRCh37.p13First PassNC_000001.10Chr165,054,48965,054,533

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)
nssv16904515<0.00126402
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