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nsv5414720

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,164

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 524 SVs from 66 studies. See in: genome view    
Submitted genomic25,340,000-25,405,163Question Mark
Overlapping variant regions from other studies: 524 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):25,666,491-25,731,654Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5414720Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr125,340,00025,405,163
nsv5414720RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr125,666,49125,731,654

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16900202duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16900202Submitted genomicNC_000001.11:g.253
40000_25405163dup
GRCh38 (hg38)NC_000001.11Chr125,340,00025,405,163
nssv16900202RemappedPerfectNC_000001.10:g.256
66491_25731654dup
GRCh37.p13First PassNC_000001.10Chr125,666,49125,731,654

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)
nssv16900202<0.00126370
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