nsv5514148

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:450

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 85 SVs from 23 studies. See in: genome view    
Submitted genomic48,940,457-48,940,906Question Mark
Overlapping variant regions from other studies: 85 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):49,443,714-49,444,163Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5514148Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1948,940,45748,940,906
nsv5514148RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,443,71449,444,163

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723940duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723940Submitted genomicNC_000019.10:g.489
40457_48940906dup
GRCh38 (hg38)NC_000019.10Chr1948,940,45748,940,906
nssv17723940RemappedPerfectNC_000019.9:g.4944
3714_49444163dup
GRCh37.p13First PassNC_000019.9Chr1949,443,71449,444,163

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)
nssv177239400.005316404
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