U.S. flag

An official website of the United States government

nsv5449817

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:834

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 214 SVs from 48 studies. See in: genome view    
Submitted genomic207,119,017-207,119,850Question Mark
Overlapping variant regions from other studies: 218 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):207,292,362-207,293,195Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449817Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1207,119,017207,119,850
nsv5449817RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1207,292,362207,293,195

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16894972deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16894972Submitted genomicNC_000001.11:g.207
119017_207119850de
l
GRCh38 (hg38)NC_000001.11Chr1207,119,017207,119,850
nssv16894972RemappedPerfectNC_000001.10:g.207
292362_207293195de
l
GRCh37.p13First PassNC_000001.10Chr1207,292,362207,293,195

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)
nssv168949720.57736946404
Support Center