nsv5560649

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 139 SVs from 30 studies. See in: genome view    
Submitted genomic78,335,230-78,335,314Question Mark
Overlapping variant regions from other studies: 139 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):78,800,914-78,800,998Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5560649Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr178,335,23078,335,314
nsv5560649RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr178,800,91478,800,998

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16905145line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16905145Submitted genomicNC_000001.11:g.783
35230_78335314ins4
527
GRCh38 (hg38)NC_000001.11Chr178,335,23078,335,314
nssv16905145RemappedPerfectNC_000001.10:g.788
00914_78800998ins4
527
GRCh37.p13First PassNC_000001.10Chr178,800,91478,800,998

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)
nssv16905145<0.00116404
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