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nsv5325418

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,093

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 239 SVs from 66 studies. See in: genome view    
Submitted genomic218,009,160-218,015,252Question Mark
Overlapping variant regions from other studies: 245 SVs from 66 studies. See in: genome view    
Remapped(Score: Perfect):218,182,502-218,188,594Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5325418Submitted genomicGRCh38.p13Primary AssemblyNC_000001.11Chr1218,009,160218,015,252
nsv5325418RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1218,182,502218,188,594

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16736912line1 deletionSequencingSplit read and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16736912Submitted genomicNC_000001.11:g.218
009160_218015252de
l
GRCh38.p13NC_000001.11Chr1218,009,160218,015,252
nssv16736912RemappedPerfectNC_000001.10:g.218
182502_218188594de
l
GRCh37.p13First PassNC_000001.10Chr1218,182,502218,188,594

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)
nssv167369120.831
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