U.S. flag

An official website of the United States government

nsv5548254

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 25 studies. See in: genome view    
Submitted genomic58,773,551-58,773,602Question Mark
Overlapping variant regions from other studies: 115 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):59,065,750-59,065,801Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5548254Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1558,773,55158,773,602
nsv5548254RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1559,065,75059,065,801

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17700914insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17700914Submitted genomicNC_000015.10:g.587
73551_58773602ins3
27
GRCh38 (hg38)NC_000015.10Chr1558,773,55158,773,602
nssv17700914RemappedPerfectNC_000015.9:g.5906
5750_59065801ins32
7
GRCh37.p13First PassNC_000015.9Chr1559,065,75059,065,801

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)
nssv177009140.00196404
Support Center