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nsv5433015

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 21 studies. See in: genome view    
Submitted genomic160,070,221-160,070,285Question Mark
Overlapping variant regions from other studies: 117 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):160,040,011-160,040,075Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5433015Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1160,070,221160,070,285
nsv5433015RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,040,011160,040,075

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16891349deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16891349Submitted genomicNC_000001.11:g.160
070221_160070285de
l
GRCh38 (hg38)NC_000001.11Chr1160,070,221160,070,285
nssv16891349RemappedPerfectNC_000001.10:g.160
040011_160040075de
l
GRCh37.p13First PassNC_000001.10Chr1160,040,011160,040,075

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)
nssv16891349<0.00116404
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