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nsv2800976

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,553

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 296 SVs from 60 studies. See in: genome view    
Submitted genomic207,538,097-207,556,649Question Mark
Overlapping variant regions from other studies: 302 SVs from 60 studies. See in: genome view    
Remapped(Score: Perfect):207,711,442-207,729,994Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv2800976Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1207,538,097207,556,649
nsv2800976RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1207,711,442207,729,994

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13678816deletionSequencingGenotyping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv13678816Submitted genomicNC_000001.11:g.207
538097_207556649de
l18553
GRCh38 (hg38)NC_000001.11Chr1207,538,097207,556,649
nssv13678816RemappedPerfectNC_000001.10:g.207
711442_207729994de
l18553
GRCh37.p13First PassNC_000001.10Chr1207,711,442207,729,994

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)
nssv136788160.7784254
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