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nsv5563470

  • 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: 95 SVs from 20 studies. See in: genome view    
Submitted genomic100,029,035-100,029,086Question Mark
Overlapping variant regions from other studies: 95 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):100,495,372-100,495,423Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563470Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr14100,029,035100,029,086
nsv5563470RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr14100,495,372100,495,423

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17697369line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17697369Submitted genomicNC_000014.9:g.1000
29035_100029086ins
6019
GRCh38 (hg38)NC_000014.9Chr14100,029,035100,029,086
nssv17697369RemappedPerfectNC_000014.8:g.1004
95372_100495423ins
6019
GRCh37.p13First PassNC_000014.8Chr14100,495,372100,495,423

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)
nssv17697369<0.00126404
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