U.S. flag

An official website of the United States government

nsv5554463

  • 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: 102 SVs from 21 studies. See in: genome view    
Submitted genomic64,514,533-64,514,584Question Mark
Overlapping variant regions from other studies: 102 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):64,500,209-64,500,260Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5554463Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr364,514,53364,514,584
nsv5554463RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr364,500,20964,500,260

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933923line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933923Submitted genomicNC_000003.12:g.645
14533_64514584ins7
9
GRCh38 (hg38)NC_000003.12Chr364,514,53364,514,584
nssv16933923RemappedPerfectNC_000003.11:g.645
00209_64500260ins7
9
GRCh37.p13First PassNC_000003.11Chr364,500,20964,500,260

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)
nssv169339230.00186392
Support Center