U.S. flag

An official website of the United States government

nsv5518104

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85,846

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 515 SVs from 67 studies. See in: genome view    
Submitted genomic44,917,155-45,003,000Question Mark
Overlapping variant regions from other studies: 515 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):45,209,353-45,295,198Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518104Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1544,917,15545,003,000
nsv5518104RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1545,209,35345,295,198

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17701639duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17701639Submitted genomicNC_000015.10:g.449
17155_45003000dup
GRCh38 (hg38)NC_000015.10Chr1544,917,15545,003,000
nssv17701639RemappedPerfectNC_000015.9:g.4520
9353_45295198dup
GRCh37.p13First PassNC_000015.9Chr1545,209,35345,295,198

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)
nssv177016390.002126402
Support Center