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nsv5484240

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:366

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 76 SVs from 19 studies. See in: genome view    
Submitted genomic42,043,385-42,043,750Question Mark
Overlapping variant regions from other studies: 76 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):42,082,984-42,083,349Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5484240Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr742,043,38542,043,750
nsv5484240RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr742,082,98442,083,349

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16995214deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16995214Submitted genomicNC_000007.14:g.420
43385_42043750del
GRCh38 (hg38)NC_000007.14Chr742,043,38542,043,750
nssv16995214RemappedPerfectNC_000007.13:g.420
82984_42083349del
GRCh37.p13First PassNC_000007.13Chr742,082,98442,083,349

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)
nssv16995214<0.00126404
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