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nsv5448868

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:106

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 178 SVs from 27 studies. See in: genome view    
Submitted genomic236,478,259-236,478,364Question Mark
Overlapping variant regions from other studies: 181 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):236,641,559-236,641,664Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5448868Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1236,478,259236,478,364
nsv5448868RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1236,641,559236,641,664

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16898744deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16898744Submitted genomicNC_000001.11:g.236
478259_236478364de
l
GRCh38 (hg38)NC_000001.11Chr1236,478,259236,478,364
nssv16898744RemappedPerfectNC_000001.10:g.236
641559_236641664de
l
GRCh37.p13First PassNC_000001.10Chr1236,641,559236,641,664

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)
nssv168987440.002126404
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