U.S. flag

An official website of the United States government

nsv5414205

  • 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: 313 SVs from 20 studies. See in: genome view    
Submitted genomic70,340,621-70,340,672Question Mark
Overlapping variant regions from other studies: 313 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):68,007,857-68,007,908Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5414205Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1870,340,62170,340,672
nsv5414205RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1868,007,85768,007,908

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17719225alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17719225Submitted genomicNC_000018.10:g.703
40621_70340672ins2
80
GRCh38 (hg38)NC_000018.10Chr1870,340,62170,340,672
nssv17719225RemappedPerfectNC_000018.9:g.6800
7857_68007908ins28
0
GRCh37.p13First PassNC_000018.9Chr1868,007,85768,007,908

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)
nssv177192250.002156404
Support Center