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nsv5424782

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:96

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 141 SVs from 27 studies. See in: genome view    
Submitted genomic14,185,297-14,185,392Question Mark
Overlapping variant regions from other studies: 141 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):14,088,614-14,088,709Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424782Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1714,185,29714,185,392
nsv5424782RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1714,088,61414,088,709

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17711606alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17711606Submitted genomicNC_000017.11:g.141
85297_14185392ins2
79
GRCh38 (hg38)NC_000017.11Chr1714,185,29714,185,392
nssv17711606RemappedPerfectNC_000017.10:g.140
88614_14088709ins2
79
GRCh37.p13First PassNC_000017.10Chr1714,088,61414,088,709

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)
nssv177116060.008526404
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