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nsv5553393

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:34

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 117 SVs from 23 studies. See in: genome view    
Submitted genomic194,641,883-194,641,916Question Mark
Overlapping variant regions from other studies: 117 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):194,362,612-194,362,645Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5553393Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3194,641,883194,641,916
nsv5553393RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3194,362,612194,362,645

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16944549insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16944549Submitted genomicNC_000003.12:g.194
641883_194641916in
s321
GRCh38 (hg38)NC_000003.12Chr3194,641,883194,641,916
nssv16944549RemappedPerfectNC_000003.11:g.194
362612_194362645in
s321
GRCh37.p13First PassNC_000003.11Chr3194,362,612194,362,645

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)
nssv169445490.0181186404
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