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nsv5442704

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:77

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 18 studies. See in: genome view    
Submitted genomic226,757,407-226,757,483Question Mark
Overlapping variant regions from other studies: 97 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):227,622,123-227,622,199Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5442704Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2226,757,407226,757,483
nsv5442704RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2227,622,123227,622,199

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16924011deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16924011Submitted genomicNC_000002.12:g.226
757407_226757483de
l
GRCh38 (hg38)NC_000002.12Chr2226,757,407226,757,483
nssv16924011RemappedPerfectNC_000002.11:g.227
622123_227622199de
l
GRCh37.p13First PassNC_000002.11Chr2227,622,123227,622,199

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)
nssv169240110.00176404
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