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nsv5441024

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,843

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 90 SVs from 22 studies. See in: genome view    
Submitted genomic44,909,778-44,916,620Question Mark
Overlapping variant regions from other studies: 90 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):44,951,270-44,958,112Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5441024Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr344,909,77844,916,620
nsv5441024RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr344,951,27044,958,112

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933673duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933673Submitted genomicNC_000003.12:g.449
09778_44916620dup
GRCh38 (hg38)NC_000003.12Chr344,909,77844,916,620
nssv16933673RemappedPerfectNC_000003.11:g.449
51270_44958112dup
GRCh37.p13First PassNC_000003.11Chr344,951,27044,958,112

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)
nssv16933673<0.00116404
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