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nsv5435475

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:62

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 84 SVs from 16 studies. See in: genome view    
Submitted genomic182,874,783-182,874,844Question Mark
Overlapping variant regions from other studies: 84 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):182,592,571-182,592,632Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5435475Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3182,874,783182,874,844
nsv5435475RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3182,592,571182,592,632

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16942545deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16942545Submitted genomicNC_000003.12:g.182
874783_182874844de
l
GRCh38 (hg38)NC_000003.12Chr3182,874,783182,874,844
nssv16942545RemappedPerfectNC_000003.11:g.182
592571_182592632de
l
GRCh37.p13First PassNC_000003.11Chr3182,592,571182,592,632

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)
nssv16942545<0.00116404
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