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nsv5413989

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,322

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 130 SVs from 30 studies. See in: genome view    
Submitted genomic155,020,589-155,021,910Question Mark
Overlapping variant regions from other studies: 137 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):154,993,065-154,994,386Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5413989Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1155,020,589155,021,910
nsv5413989RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1154,993,065154,994,386

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890424deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890424Submitted genomicNC_000001.11:g.155
020589_155021910de
l
GRCh38 (hg38)NC_000001.11Chr1155,020,589155,021,910
nssv16890424RemappedPerfectNC_000001.10:g.154
993065_154994386de
l
GRCh37.p13First PassNC_000001.10Chr1154,993,065154,994,386

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)
nssv168904240.005316402
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