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nsv5437023

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:389

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 19 studies. See in: genome view    
Submitted genomic127,574,657-127,575,045Question Mark
Overlapping variant regions from other studies: 98 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):127,293,500-127,293,888Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5437023Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3127,574,657127,575,045
nsv5437023RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3127,293,500127,293,888

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16939563duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16939563Submitted genomicNC_000003.12:g.127
574657_127575045du
p
GRCh38 (hg38)NC_000003.12Chr3127,574,657127,575,045
nssv16939563RemappedPerfectNC_000003.11:g.127
293500_127293888du
p
GRCh37.p13First PassNC_000003.11Chr3127,293,500127,293,888

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)
nssv16939563<0.00126404
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