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nsv5465699

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:63

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 125 SVs from 26 studies. See in: genome view    
Submitted genomic109,564,870-109,564,932Question Mark
Overlapping variant regions from other studies: 125 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):109,886,073-109,886,135Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5465699Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6109,564,870109,564,932
nsv5465699RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6109,886,073109,886,135

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16986390deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16986390Submitted genomicNC_000006.12:g.109
564870_109564932de
l
GRCh38 (hg38)NC_000006.12Chr6109,564,870109,564,932
nssv16986390RemappedPerfectNC_000006.11:g.109
886073_109886135de
l
GRCh37.p13First PassNC_000006.11Chr6109,886,073109,886,135

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)
nssv16986390<0.00116404
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