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nsv5564107

  • 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: 129 SVs from 22 studies. See in: genome view    
Submitted genomic24,812,304-24,812,355Question Mark
Overlapping variant regions from other studies: 129 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):25,035,173-25,035,224Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5564107Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr224,812,30424,812,355
nsv5564107RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr225,035,17325,035,224

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16910571sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16910571Submitted genomicNC_000002.12:g.248
12304_24812355ins4
67
GRCh38 (hg38)NC_000002.12Chr224,812,30424,812,355
nssv16910571RemappedPerfectNC_000002.11:g.250
35173_25035224ins4
67
GRCh37.p13First PassNC_000002.11Chr225,035,17325,035,224

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)
nssv16910571<0.00146404
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