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nsv5473684

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:160

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 122 SVs from 23 studies. See in: genome view    
Submitted genomic135,630,252-135,630,411Question Mark
Overlapping variant regions from other studies: 122 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):135,951,390-135,951,549Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5473684Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6135,630,252135,630,411
nsv5473684RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6135,951,390135,951,549

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16970792deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16970792Submitted genomicNC_000006.12:g.135
630252_135630411de
l
GRCh38 (hg38)NC_000006.12Chr6135,630,252135,630,411
nssv16970792RemappedPerfectNC_000006.11:g.135
951390_135951549de
l
GRCh37.p13First PassNC_000006.11Chr6135,951,390135,951,549

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)
nssv16970792<0.00116404
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