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nsv5451614

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,013

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 109 SVs from 22 studies. See in: genome view    
Submitted genomic127,742,554-127,743,566Question Mark
Overlapping variant regions from other studies: 109 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):127,461,397-127,462,409Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5451614Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3127,742,554127,743,566
nsv5451614RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3127,461,397127,462,409

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16939569deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16939569Submitted genomicNC_000003.12:g.127
742554_127743566de
l
GRCh38 (hg38)NC_000003.12Chr3127,742,554127,743,566
nssv16939569RemappedPerfectNC_000003.11:g.127
461397_127462409de
l
GRCh37.p13First PassNC_000003.11Chr3127,461,397127,462,409

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)
nssv16939569<0.00116404
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