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nsv5455523

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,161

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 140 SVs from 39 studies. See in: genome view    
Submitted genomic73,399,955-73,404,115Question Mark
Overlapping variant regions from other studies: 140 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):74,265,672-74,269,832Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5455523Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr473,399,95573,404,115
nsv5455523RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr474,265,67274,269,832

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16952248deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16952248Submitted genomicNC_000004.12:g.733
99955_73404115del
GRCh38 (hg38)NC_000004.12Chr473,399,95573,404,115
nssv16952248RemappedPerfectNC_000004.11:g.742
65672_74269832del
GRCh37.p13First PassNC_000004.11Chr474,265,67274,269,832

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)
nssv16952248<0.00126404
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