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nsv5441229

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:259

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 187 SVs from 36 studies. See in: genome view    
Submitted genomic169,554,497-169,554,755Question Mark
Overlapping variant regions from other studies: 187 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):170,411,007-170,411,265Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5441229Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2169,554,497169,554,755
nsv5441229RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2170,411,007170,411,265

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17730041deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17730041Submitted genomicNC_000002.12:g.169
554497_169554755de
l
GRCh38 (hg38)NC_000002.12Chr2169,554,497169,554,755
nssv17730041RemappedPerfectNC_000002.11:g.170
411007_170411265de
l
GRCh37.p13First PassNC_000002.11Chr2170,411,007170,411,265

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)
nssv177300410.0674046040
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