nsv5504663

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:101

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 139 SVs from 21 studies. See in: genome view    
Submitted genomic122,814,204-122,814,304Question Mark
Overlapping variant regions from other studies: 139 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):122,684,912-122,685,012Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5504663Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11122,814,204122,814,304
nsv5504663RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11122,684,912122,685,012

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17053331deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17053331Submitted genomicNC_000011.10:g.122
814204_122814304de
l
GRCh38 (hg38)NC_000011.10Chr11122,814,204122,814,304
nssv17053331RemappedPerfectNC_000011.9:g.1226
84912_122685012del
GRCh37.p13First PassNC_000011.9Chr11122,684,912122,685,012

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)
nssv17053331<0.00116404
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