U.S. flag

An official website of the United States government

nsv5450787

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:63

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 18 studies. See in: genome view    
Submitted genomic179,110,121-179,110,183Question Mark
Overlapping variant regions from other studies: 91 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):178,827,909-178,827,971Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5450787Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3179,110,121179,110,183
nsv5450787RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3178,827,909178,827,971

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16942997deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16942997Submitted genomicNC_000003.12:g.179
110121_179110183de
l
GRCh38 (hg38)NC_000003.12Chr3179,110,121179,110,183
nssv16942997RemappedPerfectNC_000003.11:g.178
827909_178827971de
l
GRCh37.p13First PassNC_000003.11Chr3178,827,909178,827,971

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)
nssv16942997<0.00116404
Support Center