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nsv5439171

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,086,318

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 3505 SVs from 83 studies. See in: genome view    
Submitted genomic46,970,724-48,057,041Question Mark
Overlapping variant regions from other studies: 3505 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):47,197,863-48,284,180Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5439171Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr246,970,72448,057,041
nsv5439171RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr247,197,86348,284,180

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16913276duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16913276Submitted genomicNC_000002.12:g.469
70724_48057041dup
GRCh38 (hg38)NC_000002.12Chr246,970,72448,057,041
nssv16913276RemappedPerfectNC_000002.11:g.471
97863_48284180dup
GRCh37.p13First PassNC_000002.11Chr247,197,86348,284,180

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)
nssv16913276<0.00116404
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