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nsv5443435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:739

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 334 SVs from 53 studies. See in: genome view    
Submitted genomic196,334,885-196,335,623Question Mark
Overlapping variant regions from other studies: 334 SVs from 53 studies. See in: genome view    
Remapped(Score: Perfect):196,061,756-196,062,494Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5443435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3196,334,885196,335,623
nsv5443435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3196,061,756196,062,494

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16944622deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16944622Submitted genomicNC_000003.12:g.196
334885_196335623de
l
GRCh38 (hg38)NC_000003.12Chr3196,334,885196,335,623
nssv16944622RemappedPerfectNC_000003.11:g.196
061756_196062494de
l
GRCh37.p13First PassNC_000003.11Chr3196,061,756196,062,494

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)
nssv16944622<0.00166404
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