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nsv5548318

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:17

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 100 SVs from 21 studies. See in: genome view    
Submitted genomic171,019,164-171,019,180Question Mark
Overlapping variant regions from other studies: 100 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):170,736,953-170,736,969Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5548318Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3171,019,164171,019,180
nsv5548318RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3170,736,953170,736,969

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17735010insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17735010Submitted genomicNC_000003.12:g.171
019164_171019180in
s51
GRCh38 (hg38)NC_000003.12Chr3171,019,164171,019,180
nssv17735010RemappedPerfectNC_000003.11:g.170
736953_170736969in
s51
GRCh37.p13First PassNC_000003.11Chr3170,736,953170,736,969

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)
nssv17735010<0.00126404
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