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nsv5547408

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:38

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 127 SVs from 32 studies. See in: genome view    
Submitted genomic30,639,175-30,639,212Question Mark
Overlapping variant regions from other studies: 127 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):30,606,952-30,606,989Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5547408Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr630,639,17530,639,212
nsv5547408RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr630,606,95230,606,989

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16983445insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16983445Submitted genomicNC_000006.12:g.306
39175_30639212ins3
36
GRCh38 (hg38)NC_000006.12Chr630,639,17530,639,212
nssv16983445RemappedPerfectNC_000006.11:g.306
06952_30606989ins3
36
GRCh37.p13First PassNC_000006.11Chr630,606,95230,606,989

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)
nssv16983445<0.00116404
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