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nsv5436828

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:668

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 128 SVs from 17 studies. See in: genome view    
Submitted genomic226,557,606-226,558,273Question Mark
Overlapping variant regions from other studies: 131 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):226,745,307-226,745,974Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5436828Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1226,557,606226,558,273
nsv5436828RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1226,745,307226,745,974

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16896835deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16896835Submitted genomicNC_000001.11:g.226
557606_226558273de
l
GRCh38 (hg38)NC_000001.11Chr1226,557,606226,558,273
nssv16896835RemappedPerfectNC_000001.10:g.226
745307_226745974de
l
GRCh37.p13First PassNC_000001.10Chr1226,745,307226,745,974

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)
nssv16896835<0.00126404
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