U.S. flag

An official website of the United States government

nsv4249025

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:934

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 70 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):74,898,819-74,899,752Question Mark
Overlapping variant regions from other studies: 70 SVs from 7 studies. See in: genome view    
Submitted genomic75,191,160-75,192,093Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4249025RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1574,898,81974,899,752
nsv4249025Submitted genomicGRCh37.p13Primary AssemblyNC_000015.9Chr1575,191,16075,192,093

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15826196deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15826196RemappedPerfectNC_000015.10:g.748
98819_74899752del
GRCh38.p12First PassNC_000015.10Chr1574,898,81974,899,752
nssv15826196Submitted genomicNC_000015.9:g.7519
1160_75192093del
GRCh37.p13NC_000015.9Chr1575,191,16075,192,093

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)
nssv158261964.6e-005121694
Support Center