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nsv5564055

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 140 SVs from 30 studies. See in: genome view    
Submitted genomic14,957,154-14,957,205Question Mark
Overlapping variant regions from other studies: 141 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):15,110,088-15,110,139Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5564055Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1214,957,15414,957,205
nsv5564055RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1215,110,08815,110,139

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17054268line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17054268Submitted genomicNC_000012.12:g.149
57154_14957205ins1
324
GRCh38 (hg38)NC_000012.12Chr1214,957,15414,957,205
nssv17054268RemappedPerfectNC_000012.11:g.151
10088_15110139ins1
324
GRCh37.p13First PassNC_000012.11Chr1215,110,08815,110,139

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)
nssv17054268<0.00116404
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