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nsv5427275

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,088

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 32 studies. See in: genome view    
Submitted genomic58,538,768-58,549,855Question Mark
Overlapping variant regions from other studies: 153 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):59,004,440-59,015,527Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5427275Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr158,538,76858,549,855
nsv5427275RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr159,004,44059,015,527

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16903834duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16903834Submitted genomicNC_000001.11:g.585
38768_58549855dup
GRCh38 (hg38)NC_000001.11Chr158,538,76858,549,855
nssv16903834RemappedPerfectNC_000001.10:g.590
04440_59015527dup
GRCh37.p13First PassNC_000001.10Chr159,004,44059,015,527

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)
nssv16903834<0.00116404
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