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nsv5549707

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 26 studies. See in: genome view    
Submitted genomic75,495,820-75,495,820Question Mark
Overlapping variant regions from other studies: 115 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):75,889,600-75,889,600Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5549707Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1275,495,82075,495,820
nsv5549707RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1275,889,60075,889,600

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17689228insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17689228Submitted genomicNC_000012.12:g.754
95820_75495821ins3
25
GRCh38 (hg38)NC_000012.12Chr1275,495,82075,495,820
nssv17689228RemappedPerfectNC_000012.11:g.758
89600_75889601ins3
25
GRCh37.p13First PassNC_000012.11Chr1275,889,60075,889,600

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)
nssv176892280.005315658
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