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nsv5931964

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:104

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 150 SVs from 29 studies. See in: genome view    
Submitted genomic78,397,289-78,397,392Question Mark
Overlapping variant regions from other studies: 150 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):76,393,370-76,393,473Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5931964Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1778,397,28978,397,392
nsv5931964RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1776,393,37076,393,473

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17387729duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17387729Submitted genomicNC_000017.11:g.783
97289_78397392dup
GRCh38 (hg38)NC_000017.11Chr1778,397,28978,397,392
nssv17387729RemappedPerfectNC_000017.10:g.763
93370_76393473dup
GRCh37.p13First PassNC_000017.10Chr1776,393,37076,393,473

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)
nssv173877290.0791051330
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