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nsv5533058

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:89

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 86 SVs from 18 studies. See in: genome view    
Submitted genomic46,021,729-46,021,817Question Mark
Overlapping variant regions from other studies: 86 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):46,524,987-46,525,075Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533058Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1946,021,72946,021,817
nsv5533058RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1946,524,98746,525,075

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723620deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723620Submitted genomicNC_000019.10:g.460
21729_46021817del
GRCh38 (hg38)NC_000019.10Chr1946,021,72946,021,817
nssv17723620RemappedPerfectNC_000019.9:g.4652
4987_46525075del
GRCh37.p13First PassNC_000019.9Chr1946,524,98746,525,075

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)
nssv17723620<0.00116404
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